Physical health problems in adults with Prader-Willi syndrome

Prader–Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and adolescence, this is followed by hyperphagia and extreme obesity if the diet is not strictly controlled. Data on physical health problems in adul...

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Published inAmerican journal of medical genetics. Part A Vol. 155A; no. 9; pp. 2112 - 2124
Main Authors Sinnema, Margje, Maaskant, Marian A., van Schrojenstein Lantman-de Valk, Henny M.J., Caroline van Nieuwpoort, I., Drent, Madeleine L., Curfs, Leopold M.G., Schrander-Stumpel, Constance T.R.M.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.09.2011
Wiley-Liss
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ISSN1552-4825
1552-4833
1552-4833
DOI10.1002/ajmg.a.34171

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Abstract Prader–Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and adolescence, this is followed by hyperphagia and extreme obesity if the diet is not strictly controlled. Data on physical health problems in adults with PWS are scarce. We report on the prevalence of physical health problems in a Dutch cohort of adults with PWS in relation to age, BMI, and genetic subtype. Participants (n = 102) were retrieved via the Dutch Prader–Willi Parent Association and through physicians specializing in persons with intellectual disabilities (ID). Details regarding physical health problem spanning the participants' lifespan were collected from caretakers through semi‐structured interviews. Cardiovascular problems included diabetes mellitus, hypertension, and cerebrovascular accidents. Respiratory infections were frequent in adulthood. In males, cryptorchidism was almost universal, for which 28/48 males had a history of surgery, mostly orchidopexy. None of the women had a regular menstrual cycle. Sixteen individuals had a diagnosis of osteoporosis. Spinal deformation, hip dysplasia, and foot abnormalities were common. Skinpicking, leg edema, and erysipelas were frequent dermatological problems. The findings in our group support the notion that the prevalence of physical health problems is underestimated. This underscores the importance of developing monitoring programs which would help to recognize physical health problems at an early stage. © 2011 Wiley‐Liss, Inc.
AbstractList Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and adolescence, this is followed by hyperphagia and extreme obesity if the diet is not strictly controlled. Data on physical health problems in adults with PWS are scarce. We report on the prevalence of physical health problems in a Dutch cohort of adults with PWS in relation to age, BMI, and genetic subtype. Participants (n = 102) were retrieved via the Dutch Prader-Willi Parent Association and through physicians specializing in persons with intellectual disabilities (ID). Details regarding physical health problem spanning the participants' lifespan were collected from caretakers through semi-structured interviews. Cardiovascular problems included diabetes mellitus, hypertension, and cerebrovascular accidents. Respiratory infections were frequent in adulthood. In males, cryptorchidism was almost universal, for which 28/48 males had a history of surgery, mostly orchidopexy. None of the women had a regular menstrual cycle. Sixteen individuals had a diagnosis of osteoporosis. Spinal deformation, hip dysplasia, and foot abnormalities were common. Skinpicking, leg edema, and erysipelas were frequent dermatological problems. The findings in our group support the notion that the prevalence of physical health problems is underestimated. This underscores the importance of developing monitoring programs which would help to recognize physical health problems at an early stage.Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and adolescence, this is followed by hyperphagia and extreme obesity if the diet is not strictly controlled. Data on physical health problems in adults with PWS are scarce. We report on the prevalence of physical health problems in a Dutch cohort of adults with PWS in relation to age, BMI, and genetic subtype. Participants (n = 102) were retrieved via the Dutch Prader-Willi Parent Association and through physicians specializing in persons with intellectual disabilities (ID). Details regarding physical health problem spanning the participants' lifespan were collected from caretakers through semi-structured interviews. Cardiovascular problems included diabetes mellitus, hypertension, and cerebrovascular accidents. Respiratory infections were frequent in adulthood. In males, cryptorchidism was almost universal, for which 28/48 males had a history of surgery, mostly orchidopexy. None of the women had a regular menstrual cycle. Sixteen individuals had a diagnosis of osteoporosis. Spinal deformation, hip dysplasia, and foot abnormalities were common. Skinpicking, leg edema, and erysipelas were frequent dermatological problems. The findings in our group support the notion that the prevalence of physical health problems is underestimated. This underscores the importance of developing monitoring programs which would help to recognize physical health problems at an early stage.
Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and adolescence, this is followed by hyperphagia and extreme obesity if the diet is not strictly controlled. Data on physical health problems in adults with PWS are scarce. We report on the prevalence of physical health problems in a Dutch cohort of adults with PWS in relation to age, BMI, and genetic subtype. Participants (n=102) were retrieved via the Dutch Prader-Willi Parent Association and through physicians specializing in persons with intellectual disabilities (ID). Details regarding physical health problem spanning the participants' lifespan were collected from caretakers through semi-structured interviews. Cardiovascular problems included diabetes mellitus, hypertension, and cerebrovascular accidents. Respiratory infections were frequent in adulthood. In males, cryptorchidism was almost universal, for which 28/48 males had a history of surgery, mostly orchidopexy. None of the women had a regular menstrual cycle. Sixteen individuals had a diagnosis of osteoporosis. Spinal deformation, hip dysplasia, and foot abnormalities were common. Skinpicking, leg edema, and erysipelas were frequent dermatological problems. The findings in our group support the notion that the prevalence of physical health problems is underestimated. This underscores the importance of developing monitoring programs which would help to recognize physical health problems at an early stage. ? 2011 Wiley-Liss, Inc.
Prader–Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and adolescence, this is followed by hyperphagia and extreme obesity if the diet is not strictly controlled. Data on physical health problems in adults with PWS are scarce. We report on the prevalence of physical health problems in a Dutch cohort of adults with PWS in relation to age, BMI, and genetic subtype. Participants (n = 102) were retrieved via the Dutch Prader–Willi Parent Association and through physicians specializing in persons with intellectual disabilities (ID). Details regarding physical health problem spanning the participants' lifespan were collected from caretakers through semi‐structured interviews. Cardiovascular problems included diabetes mellitus, hypertension, and cerebrovascular accidents. Respiratory infections were frequent in adulthood. In males, cryptorchidism was almost universal, for which 28/48 males had a history of surgery, mostly orchidopexy. None of the women had a regular menstrual cycle. Sixteen individuals had a diagnosis of osteoporosis. Spinal deformation, hip dysplasia, and foot abnormalities were common. Skinpicking, leg edema, and erysipelas were frequent dermatological problems. The findings in our group support the notion that the prevalence of physical health problems is underestimated. This underscores the importance of developing monitoring programs which would help to recognize physical health problems at an early stage. © 2011 Wiley‐Liss, Inc.
Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and adolescence, this is followed by hyperphagia and extreme obesity if the diet is not strictly controlled. Data on physical health problems in adults with PWS are scarce. We report on the prevalence of physical health problems in a Dutch cohort of adults with PWS in relation to age, BMI, and genetic subtype. Participants (n = 102) were retrieved via the Dutch Prader-Willi Parent Association and through physicians specializing in persons with intellectual disabilities (ID). Details regarding physical health problem spanning the participants' lifespan were collected from caretakers through semi-structured interviews. Cardiovascular problems included diabetes mellitus, hypertension, and cerebrovascular accidents. Respiratory infections were frequent in adulthood. In males, cryptorchidism was almost universal, for which 28/48 males had a history of surgery, mostly orchidopexy. None of the women had a regular menstrual cycle. Sixteen individuals had a diagnosis of osteoporosis. Spinal deformation, hip dysplasia, and foot abnormalities were common. Skinpicking, leg edema, and erysipelas were frequent dermatological problems. The findings in our group support the notion that the prevalence of physical health problems is underestimated. This underscores the importance of developing monitoring programs which would help to recognize physical health problems at an early stage.
Author Schrander-Stumpel, Constance T.R.M.
van Schrojenstein Lantman-de Valk, Henny M.J.
Maaskant, Marian A.
Curfs, Leopold M.G.
Drent, Madeleine L.
Sinnema, Margje
Caroline van Nieuwpoort, I.
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  surname: van Schrojenstein Lantman-de Valk
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  surname: Caroline van Nieuwpoort
  fullname: Caroline van Nieuwpoort, I.
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  givenname: Madeleine L.
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Issue 9
Keywords Endocrinopathy
Human
Handicap
Prader-Willi syndrome
Health
Ageing
Diseases of the osteoarticular system
Developmental disorder
Mental retardation
Genetic disease
intellectual disabilities
physical health problems
Intellectual deficiency
Adult
Complex syndrome
Prader Labhart Willi syndrome
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
CC BY 4.0
Copyright © 2011 Wiley-Liss, Inc.
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Leopold M.G. Curfs and Constance T.R.M. Schrander-Stumpel contributed equally to this work.
Dutch Prader-Willi Fund
How to Cite this Article: Sinnema M, Maaskant MA, van Schrojenstein Lantman-de Valk HMJ, Caroline van Nieuwpoort I, Drent ML, Curfs LMG, Schrander-Stumpel CTRM. 2011. Physical Health Problems In Adults With Prader-Willi Syndrome. Am J Med Genet Part A 155:2112-2124.
Leopold M.G. Curfs and Constance T.R.M. Schrander‐Stumpel contributed equally to this work.
How to Cite this Article: Sinnema M, Maaskant MA, van Schrojenstein Lantman‐de Valk HMJ, Caroline van Nieuwpoort I, Drent ML, Curfs LMG, Schrander‐Stumpel CTRM. 2011. Physical Health Problems In Adults With Prader–Willi Syndrome. Am J Med Genet Part A 155:2112–2124.
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PublicationDate September 2011
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PublicationDate_xml – month: 09
  year: 2011
  text: September 2011
PublicationDecade 2010
PublicationPlace Hoboken
PublicationPlace_xml – name: Hoboken
– name: Chichester
– name: United States
PublicationTitle American journal of medical genetics. Part A
PublicationTitleAlternate Am. J. Med. Genet
PublicationYear 2011
Publisher Wiley Subscription Services, Inc., A Wiley Company
Wiley-Liss
Publisher_xml – name: Wiley Subscription Services, Inc., A Wiley Company
– name: Wiley-Liss
References Vogels A, De Hert M, Descheemaeker MJ, Govers V, Devriendt K, Legius E, Prinzie P, Fryns JP. 2004a Psychotic disorders in Prader-Willi syndrome. Am J Med Genet Part A 127A: 238-243.
Schulze A, Mogensen H, Hamborg-Petersen B, Graem N, Ostergaard JR, Brondum-Nielsen K. 2001. Fertility in Prader-Willi syndrome: A case report with Angelman syndrome in the offspring. Acta Paediatr 90: 455-459.
Goldstone AP. 2004. Prader-Willi syndrome: Advances in genetics, pathophysiology and treatment. Trends Endocrinol Metab 15: 12-20.
Jung BH, Jeon MJ, Bai SW. 2008. Hormone-dependent aging problems in women. Yonsei Med J 49: 345-351.
Sinnema M, Boer H, Collin P, Maaskant MA, van Roozendaal KEP, Schrander-Stumpel CTRM, Curfs LMG. 2011a Psychiatric illness in a cohort of adults with Prader-Willi syndrome. Res Dev Disabil 32: 1729-1735.
Wood HM, Elder JS. 2009. Cryptorchidism and testicular cancer: Separating fact from fiction. J Urol 181: 452-461.
Kusuhara T, Ayabe M, Hino H, Shoji H, Neshige R. 1996. A case of Prader-Willi syndrome with bilateral middle cerebral artery occlusion and moyamoya phenomenon. Rinsho Shinkeigaku 36: 770-773.
Sinnema M, Einfeld SL, Schrander-Stumpel CT, Maaskant MA, Boer H, Curfs LM. 2011b Behavioral phenotype in adults with Prader-Willi syndrome. Res Dev Disabil 32: 604-612.
Patel DR, Greydanus DE, Calles JL, Pratt HD. 2010. Developmental disabilities across the lifespan. Dis Mon 56: 304-397.
Valdovinos MG, Caruso M, Roberts C, Kim G, Kennedy CH. 2005. Medical and behavioral symptoms as potential medication side effects in adults with developmental disabilities. Am J Ment Retard 110: 164-170.
Gooren LJ. 2010. Androgens and male aging: Current evidence of safety and efficacy. Asian J Androl 12: 136-151.
Carpenter PK. 1994. Prader-Willi syndrome in old age. J Intellect Disabil Res 38: 529-531.
Hoybye C. 2007. Five-years growth hormone (GH) treatment in adults with Prader-Willi syndrome. Acta Paediatr 96: 410-413.
Charlson ME, Pompei P, Ales KL, MacKenzie CR. 1987. A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation. J Chronic Dis 40: 373-383.
Nicholls RD, Knoll JH, Butler MG, Karam S, Lalande M. 1989. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. Nature 342: 281-285.
Clark LI, O'Toole MS. 2007. Intellectual impairment and sexual health: Information needs. Br J Nurs 16: 154-156.
Robinson AC, Jones WG. 1990. Prader Willi syndrome and testicular tumour. Clin Oncol (R Coll Radiol) 2: 117.
Butler MG, Haber L, Mernaugh R, Carlson MG, Price R, Feurer ID. 2001. Decreased bone mineral density in Prader-Willi syndrome: Comparison with obese subjects. Am J Med Genet 103: 216-222.
Eiholzer U. 2005. Deaths in children with Prader-Willi syndrome. A contribution to the debate about the safety of growth hormone treatment in children with PWS Horm Res 63: 33-39.
Soni S, Whittington J, Holland AJ, Webb T, Maina E, Boer H, Clarke D. 2007. The course and outcome of psychiatric illness in people with Prader-Willi syndrome: Implications for management and treatment. J Intellect Disabil Res 51: 32-42.
Couper RT, Couper JJ. 2000. Prader-Willi syndrome. Lancet 356: 673-675.
Boer H, Holland A, Whittington J, Butler J, Webb T, Clarke D. 2002. Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy. Lancet 359: 135-136.
Kroonen LT, Herman M, Pizzutillo PD, Macewen GD. 2006. Prader-Willi Syndrome: Clinical concerns for the orthopaedic surgeon. J Pediatr Orthop 26: 673-679.
Dykens EM, Roof E. 2008. Behavior in Prader-Willi syndrome: Relationship to genetic subtypes and age. J Child Psychol Psychiatry 49: 1001-1008.
Sundararajan V, Henderson T, Perry C, Muggivan A, Quan H, Ghali WA. 2004. New ICD-10 version of the Charlson comorbidity index predicted in-hospital mortality. J Clin Epidemiol 57: 1288-1294.
Goldstone AP, Holland AJ, Hauffa BP, Hokken-Koelega AC, Tauber M. 2008. Recommendations for the diagnosis and management of Prader-Willi syndrome. J Clin Endocrinol Metab 93: 4183-4197.
Campeotto F, Naudin C, Viot G, Dupont C. 2001. Rectal self-mutilation, rectal bleeding and Prader-Willi syndrome. Arch Pediatr 8: 1075-1077.
van Schrojenstein Lantman-de Valk HM, Walsh PN. 2008. Managing health problems in people with intellectual disabilities. Br Med J 337: a2507.
Servais L. 2006. Sexual health care in persons with intellectual disabilities. Ment Retard Dev Disabil Res Rev 12: 48-56.
Butler JV, Whittington JE, Holland AJ, Boer H, Clarke D, Webb T. 2002. Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: A population-based study. Dev Med Child Neurol 44: 248-255.
Lamb AS, Johnson WM. 1987. Premature coronary artery atherosclerosis in a patient with Prader-Willi syndrome. Am J Med Genet 28: 873-880.
Akefeldt A, Tornhage CJ, Gillberg C. 1999. A woman with Prader-Willi syndrome gives birth to a healthy baby girl. Dev Med Child Neurol 41: 789-790.
van den Berg JS, Hennekam RC, Cruysberg JR, Steijlen PM, Swart J, Tijmes N, Limburg M. 2000. Prevalence of symptomatic intracranial aneurysm and ischaemic stroke in pseudoxanthoma elasticum. Cerebrovasc Dis 10: 315-319.
Jaffray B, Moore L, Dickson AP. 1999. Prader-Willi syndrome and intratubular germ cell neoplasia. Med Pediatr Oncol 32: 73-74.
Ledbetter DH, Riccardi VM, Airhart SD, Strobel RJ, Keenan BS, Crawford JD. 1981. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. N Engl J Med 304: 325-329.
Laurance BM, Brito A, Wilkinson J. 1981. Prader-Willi Syndrome after age 15 years. Arch Dis Child 56: 181-186.
Vogels A, Frijns JP. 2004b Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndrome. Genet Couns 15: 397-404.
Page SR, Nussey SS, Haywood GA, Jenkins JS. 1990. Premature coronary artery disease and the Prader-Willi syndrome. Postgrad Med J 66: 232-234.
Didden R, Korzilius H, Curfs L. 2007. Skin-picking in individuals with Prader-Willi syndrome: Prevalence, functional assessment, and its comorbidity with compulsive and self-injurious behaviours. J Appl Res Intellect Disabil 20: 409-419.
Stevenson DA, Anaya TM, Clayton-Smith J, Hall BD, Van Allen MI, Zori RT, Zackai EH, Frank G, Clericuzio CL. 2004. Unexpected death and critical illness in Prader-Willi syndrome: Report of ten individuals. Am J Med Genet Part A 124A: 158-164.
Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B. 1995. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet 9: 395-400.
Vogels A, Moerman P, Frijns JP, Bogaert GA. 2008. Testicular histology in boys with Prader-Willi syndrome: Fertile or infertile? J Urol 180: 1800-1804.
Einfeld SL, Kavanagh SJ, Smith A, Evans EJ, Tonge BJ, Taffe J. 2006. Mortality in Prader-Willi syndrome. Am J Ment Retard 111: 193-198.
Must A, Spadano J, Coakley EH, Field AE, Colditz G, Dietz WH. 1999. The disease burden associated with overweight and obesity. JAMA 282: 1523-1529.
Bhargava SA, Putnam PE, Kocoshis SA, Rowe M, Hanchett JM. 1996. Rectal bleeding in Prader-Willi syndrome. Pediatrics 97: 265-267.
Grol R, Cluzeau FA, Burgers JS. 2003. Clinical practice guidelines: Towards better quality guidelines and increased international collaboration. Br J Cancer 89: S4-S8.
Ashley RA, Barthold JS, Kolon TF. 2010. Cryptorchidism: Pathogenesis, diagnosis, treatment and prognosis. Urol Clin North Am 37: 183-193.
Holm VA, Cassidy SB, Butler MG, Hanchett JM, Greenswag LR, Whitman BY, Greenberg F. 1993. Prader-Willi syndrome: Consensus diagnostic criteria. Pediatrics 91: 398-402.
Thomson AK, Glasson EJ, Bittles AH. 2006. A long-term population-based clinical and morbidity review of Prader-Willi syndrome in Western Australia. J Intellect Disabil Res 50: 69-78.
Crino A, Schiaffini R, Ciampalini P, Spera S, Beccaria L, Benzi F, Bosio L, Corrias A, Gargantini L, Salvatoni A, Tonini G, Trifirò G, Livieri C. 2003. Hypogonadism and pubertal development in Prader-Willi syndrome. Eur J Pediatr 162: 327-333.
Whittington JE, Holland AJ, Webb T, Butler J, Clarke D, Boer H. 2001. Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region. J Med Genet 38: 792-798.
Greenswag LR. 1987. Adults with Prader-Willi syndrome: A survey of 232 cases. Dev Med Child Neurol 29: 145-152.
Heitink MV, Sinnema M, van Steensel MA, Schrander-Stumpel CT, Frank J, Curfs LM. 2008. Lymphedema in Prader-Willi syndrome. Int J Dermatol 47: 42-44.
2010; 12
2010; 56
2001; 90
2002; 359
2011a; 32
2005; 63
1981; 304
1999; 41
1996; 36
2001; 103
1987; 40
2000; 10
2002; 44
2006; 26
1989; 342
2003; 162
1994; 38
2007; 20
2003; 89
1995; 9
2004; 124A
2010; 37
2006; 50
2006; 12
2005; 110
2000; 356
2010
2009; 181
2009
1993; 91
2007; 51
2007; 96
2008; 93
1996; 97
2006; 111
2007; 16
1990; 2
2008; 180
1990; 66
2004a; 127A
2004; 15
1999; 282
2011b; 32
2008; 49
2001; 8
2004; 57
2008; 47
1999; 32
2008; 337
2004b; 15
2001; 38
1987; 28
1987; 29
1981; 56
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References_xml – reference: Einfeld SL, Kavanagh SJ, Smith A, Evans EJ, Tonge BJ, Taffe J. 2006. Mortality in Prader-Willi syndrome. Am J Ment Retard 111: 193-198.
– reference: Robinson AC, Jones WG. 1990. Prader Willi syndrome and testicular tumour. Clin Oncol (R Coll Radiol) 2: 117.
– reference: van den Berg JS, Hennekam RC, Cruysberg JR, Steijlen PM, Swart J, Tijmes N, Limburg M. 2000. Prevalence of symptomatic intracranial aneurysm and ischaemic stroke in pseudoxanthoma elasticum. Cerebrovasc Dis 10: 315-319.
– reference: Charlson ME, Pompei P, Ales KL, MacKenzie CR. 1987. A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation. J Chronic Dis 40: 373-383.
– reference: Valdovinos MG, Caruso M, Roberts C, Kim G, Kennedy CH. 2005. Medical and behavioral symptoms as potential medication side effects in adults with developmental disabilities. Am J Ment Retard 110: 164-170.
– reference: Couper RT, Couper JJ. 2000. Prader-Willi syndrome. Lancet 356: 673-675.
– reference: Page SR, Nussey SS, Haywood GA, Jenkins JS. 1990. Premature coronary artery disease and the Prader-Willi syndrome. Postgrad Med J 66: 232-234.
– reference: Schulze A, Mogensen H, Hamborg-Petersen B, Graem N, Ostergaard JR, Brondum-Nielsen K. 2001. Fertility in Prader-Willi syndrome: A case report with Angelman syndrome in the offspring. Acta Paediatr 90: 455-459.
– reference: Butler MG, Haber L, Mernaugh R, Carlson MG, Price R, Feurer ID. 2001. Decreased bone mineral density in Prader-Willi syndrome: Comparison with obese subjects. Am J Med Genet 103: 216-222.
– reference: Boer H, Holland A, Whittington J, Butler J, Webb T, Clarke D. 2002. Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy. Lancet 359: 135-136.
– reference: Bhargava SA, Putnam PE, Kocoshis SA, Rowe M, Hanchett JM. 1996. Rectal bleeding in Prader-Willi syndrome. Pediatrics 97: 265-267.
– reference: Vogels A, Moerman P, Frijns JP, Bogaert GA. 2008. Testicular histology in boys with Prader-Willi syndrome: Fertile or infertile? J Urol 180: 1800-1804.
– reference: Ledbetter DH, Riccardi VM, Airhart SD, Strobel RJ, Keenan BS, Crawford JD. 1981. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. N Engl J Med 304: 325-329.
– reference: van Schrojenstein Lantman-de Valk HM, Walsh PN. 2008. Managing health problems in people with intellectual disabilities. Br Med J 337: a2507.
– reference: Goldstone AP, Holland AJ, Hauffa BP, Hokken-Koelega AC, Tauber M. 2008. Recommendations for the diagnosis and management of Prader-Willi syndrome. J Clin Endocrinol Metab 93: 4183-4197.
– reference: Jung BH, Jeon MJ, Bai SW. 2008. Hormone-dependent aging problems in women. Yonsei Med J 49: 345-351.
– reference: Grol R, Cluzeau FA, Burgers JS. 2003. Clinical practice guidelines: Towards better quality guidelines and increased international collaboration. Br J Cancer 89: S4-S8.
– reference: Clark LI, O'Toole MS. 2007. Intellectual impairment and sexual health: Information needs. Br J Nurs 16: 154-156.
– reference: Whittington JE, Holland AJ, Webb T, Butler J, Clarke D, Boer H. 2001. Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region. J Med Genet 38: 792-798.
– reference: Crino A, Schiaffini R, Ciampalini P, Spera S, Beccaria L, Benzi F, Bosio L, Corrias A, Gargantini L, Salvatoni A, Tonini G, Trifirò G, Livieri C. 2003. Hypogonadism and pubertal development in Prader-Willi syndrome. Eur J Pediatr 162: 327-333.
– reference: Sundararajan V, Henderson T, Perry C, Muggivan A, Quan H, Ghali WA. 2004. New ICD-10 version of the Charlson comorbidity index predicted in-hospital mortality. J Clin Epidemiol 57: 1288-1294.
– reference: Sinnema M, Boer H, Collin P, Maaskant MA, van Roozendaal KEP, Schrander-Stumpel CTRM, Curfs LMG. 2011a Psychiatric illness in a cohort of adults with Prader-Willi syndrome. Res Dev Disabil 32: 1729-1735.
– reference: Ashley RA, Barthold JS, Kolon TF. 2010. Cryptorchidism: Pathogenesis, diagnosis, treatment and prognosis. Urol Clin North Am 37: 183-193.
– reference: Must A, Spadano J, Coakley EH, Field AE, Colditz G, Dietz WH. 1999. The disease burden associated with overweight and obesity. JAMA 282: 1523-1529.
– reference: Campeotto F, Naudin C, Viot G, Dupont C. 2001. Rectal self-mutilation, rectal bleeding and Prader-Willi syndrome. Arch Pediatr 8: 1075-1077.
– reference: Vogels A, De Hert M, Descheemaeker MJ, Govers V, Devriendt K, Legius E, Prinzie P, Fryns JP. 2004a Psychotic disorders in Prader-Willi syndrome. Am J Med Genet Part A 127A: 238-243.
– reference: Lamb AS, Johnson WM. 1987. Premature coronary artery atherosclerosis in a patient with Prader-Willi syndrome. Am J Med Genet 28: 873-880.
– reference: Greenswag LR. 1987. Adults with Prader-Willi syndrome: A survey of 232 cases. Dev Med Child Neurol 29: 145-152.
– reference: Didden R, Korzilius H, Curfs L. 2007. Skin-picking in individuals with Prader-Willi syndrome: Prevalence, functional assessment, and its comorbidity with compulsive and self-injurious behaviours. J Appl Res Intellect Disabil 20: 409-419.
– reference: Kroonen LT, Herman M, Pizzutillo PD, Macewen GD. 2006. Prader-Willi Syndrome: Clinical concerns for the orthopaedic surgeon. J Pediatr Orthop 26: 673-679.
– reference: Carpenter PK. 1994. Prader-Willi syndrome in old age. J Intellect Disabil Res 38: 529-531.
– reference: Holm VA, Cassidy SB, Butler MG, Hanchett JM, Greenswag LR, Whitman BY, Greenberg F. 1993. Prader-Willi syndrome: Consensus diagnostic criteria. Pediatrics 91: 398-402.
– reference: Dykens EM, Roof E. 2008. Behavior in Prader-Willi syndrome: Relationship to genetic subtypes and age. J Child Psychol Psychiatry 49: 1001-1008.
– reference: Laurance BM, Brito A, Wilkinson J. 1981. Prader-Willi Syndrome after age 15 years. Arch Dis Child 56: 181-186.
– reference: Goldstone AP. 2004. Prader-Willi syndrome: Advances in genetics, pathophysiology and treatment. Trends Endocrinol Metab 15: 12-20.
– reference: Vogels A, Frijns JP. 2004b Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndrome. Genet Couns 15: 397-404.
– reference: Hoybye C. 2007. Five-years growth hormone (GH) treatment in adults with Prader-Willi syndrome. Acta Paediatr 96: 410-413.
– reference: Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B. 1995. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet 9: 395-400.
– reference: Stevenson DA, Anaya TM, Clayton-Smith J, Hall BD, Van Allen MI, Zori RT, Zackai EH, Frank G, Clericuzio CL. 2004. Unexpected death and critical illness in Prader-Willi syndrome: Report of ten individuals. Am J Med Genet Part A 124A: 158-164.
– reference: Butler JV, Whittington JE, Holland AJ, Boer H, Clarke D, Webb T. 2002. Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: A population-based study. Dev Med Child Neurol 44: 248-255.
– reference: Gooren LJ. 2010. Androgens and male aging: Current evidence of safety and efficacy. Asian J Androl 12: 136-151.
– reference: Akefeldt A, Tornhage CJ, Gillberg C. 1999. A woman with Prader-Willi syndrome gives birth to a healthy baby girl. Dev Med Child Neurol 41: 789-790.
– reference: Servais L. 2006. Sexual health care in persons with intellectual disabilities. Ment Retard Dev Disabil Res Rev 12: 48-56.
– reference: Nicholls RD, Knoll JH, Butler MG, Karam S, Lalande M. 1989. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. Nature 342: 281-285.
– reference: Soni S, Whittington J, Holland AJ, Webb T, Maina E, Boer H, Clarke D. 2007. The course and outcome of psychiatric illness in people with Prader-Willi syndrome: Implications for management and treatment. J Intellect Disabil Res 51: 32-42.
– reference: Kusuhara T, Ayabe M, Hino H, Shoji H, Neshige R. 1996. A case of Prader-Willi syndrome with bilateral middle cerebral artery occlusion and moyamoya phenomenon. Rinsho Shinkeigaku 36: 770-773.
– reference: Sinnema M, Einfeld SL, Schrander-Stumpel CT, Maaskant MA, Boer H, Curfs LM. 2011b Behavioral phenotype in adults with Prader-Willi syndrome. Res Dev Disabil 32: 604-612.
– reference: Heitink MV, Sinnema M, van Steensel MA, Schrander-Stumpel CT, Frank J, Curfs LM. 2008. Lymphedema in Prader-Willi syndrome. Int J Dermatol 47: 42-44.
– reference: Eiholzer U. 2005. Deaths in children with Prader-Willi syndrome. A contribution to the debate about the safety of growth hormone treatment in children with PWS Horm Res 63: 33-39.
– reference: Thomson AK, Glasson EJ, Bittles AH. 2006. A long-term population-based clinical and morbidity review of Prader-Willi syndrome in Western Australia. J Intellect Disabil Res 50: 69-78.
– reference: Patel DR, Greydanus DE, Calles JL, Pratt HD. 2010. Developmental disabilities across the lifespan. Dis Mon 56: 304-397.
– reference: Wood HM, Elder JS. 2009. Cryptorchidism and testicular cancer: Separating fact from fiction. J Urol 181: 452-461.
– reference: Jaffray B, Moore L, Dickson AP. 1999. Prader-Willi syndrome and intratubular germ cell neoplasia. Med Pediatr Oncol 32: 73-74.
– year: 2009
– volume: 32
  start-page: 604
  year: 2011b
  end-page: 612
  article-title: Behavioral phenotype in adults with Prader–Willi syndrome
  publication-title: Res Dev Disabil
– volume: 36
  start-page: 770
  year: 1996
  end-page: 773
  article-title: A case of Prader–Willi syndrome with bilateral middle cerebral artery occlusion and moyamoya phenomenon
  publication-title: Rinsho Shinkeigaku
– volume: 49
  start-page: 1001
  year: 2008
  end-page: 1008
  article-title: Behavior in Prader–Willi syndrome: Relationship to genetic subtypes and age
  publication-title: J Child Psychol Psychiatry
– volume: 57
  start-page: 1288
  year: 2004
  end-page: 1294
  article-title: New ICD‐10 version of the Charlson comorbidity index predicted in‐hospital mortality
  publication-title: J Clin Epidemiol
– volume: 12
  start-page: 48
  year: 2006
  end-page: 56
  article-title: Sexual health care in persons with intellectual disabilities
  publication-title: Ment Retard Dev Disabil Res Rev
– volume: 28
  start-page: 873
  year: 1987
  end-page: 880
  article-title: Premature coronary artery atherosclerosis in a patient with Prader–Willi syndrome
  publication-title: Am J Med Genet
– volume: 359
  start-page: 135
  year: 2002
  end-page: 136
  article-title: Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy
  publication-title: Lancet
– volume: 51
  start-page: 32
  year: 2007
  end-page: 42
  article-title: The course and outcome of psychiatric illness in people with Prader–Willi syndrome: Implications for management and treatment
  publication-title: J Intellect Disabil Res
– volume: 89
  start-page: S4
  year: 2003
  end-page: S8
  article-title: Clinical practice guidelines: Towards better quality guidelines and increased international collaboration
  publication-title: Br J Cancer
– volume: 2
  start-page: 117
  year: 1990
  article-title: Prader Willi syndrome and testicular tumour
  publication-title: Clin Oncol (R Coll Radiol)
– volume: 38
  start-page: 529
  year: 1994
  end-page: 531
  article-title: Prader–Willi syndrome in old age
  publication-title: J Intellect Disabil Res
– volume: 282
  start-page: 1523
  year: 1999
  end-page: 1529
  article-title: The disease burden associated with overweight and obesity
  publication-title: JAMA
– volume: 37
  start-page: 183
  year: 2010
  end-page: 193
  article-title: Cryptorchidism: Pathogenesis, diagnosis, treatment and prognosis
  publication-title: Urol Clin North Am
– volume: 20
  start-page: 409
  year: 2007
  end-page: 419
  article-title: Skin‐picking in individuals with Prader–Willi syndrome: Prevalence, functional assessment, and its comorbidity with compulsive and self‐injurious behaviours
  publication-title: J Appl Res Intellect Disabil
– volume: 162
  start-page: 327
  year: 2003
  end-page: 333
  article-title: Hypogonadism and pubertal development in Prader–Willi syndrome
  publication-title: Eur J Pediatr
– volume: 32
  start-page: 1729
  year: 2011a
  end-page: 1735
  article-title: Psychiatric illness in a cohort of adults with Prader–Willi syndrome
  publication-title: Res Dev Disabil
– volume: 180
  start-page: 1800
  year: 2008
  end-page: 1804
  article-title: Testicular histology in boys with Prader–Willi syndrome: Fertile or infertile?
  publication-title: J Urol
– volume: 15
  start-page: 397
  year: 2004b
  end-page: 404
  article-title: Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader‐Willi syndrome
  publication-title: Genet Couns
– volume: 26
  start-page: 673
  year: 2006
  end-page: 679
  article-title: Prader–Willi Syndrome: Clinical concerns for the orthopaedic surgeon
  publication-title: J Pediatr Orthop
– volume: 66
  start-page: 232
  year: 1990
  end-page: 234
  article-title: Premature coronary artery disease and the Prader–Willi syndrome
  publication-title: Postgrad Med J
– volume: 49
  start-page: 345
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Snippet Prader–Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and...
Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and...
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SubjectTerms Adolescence
Adolescent
Adult
Adult and adolescent clinical studies
Aged
ageing
Biological and medical sciences
Body Mass Index
Children
Cohort Studies
Complex syndromes
Cryptorchidism
Cryptorchidism - complications
Data processing
Diabetes Complications
Diabetes mellitus
Diets
Edema
Erysipelas
Female
Foot
Foot Deformities, Congenital - complications
Hip Dislocation, Congenital - complications
Humans
Hyperphagia
Hypertension - complications
Infection
Intellectual deficiency
intellectual disabilities
Intellectual Disability - complications
Leg
Life span
Male
Medical genetics
Medical sciences
Menarche
Menstrual cycle
Mental retardation
Metabolic diseases
Middle Aged
Obesity
Osteoporosis
Osteoporosis - complications
physical health problems
Prader-Willi syndrome
Prader-Willi Syndrome - genetics
Prader-Willi Syndrome - physiopathology
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Respiratory Tract Infections - complications
Skin Diseases - complications
Spinal Diseases - complications
Stroke - complications
Surgery
Title Physical health problems in adults with Prader-Willi syndrome
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https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fajmg.a.34171
https://www.ncbi.nlm.nih.gov/pubmed/21834028
https://www.proquest.com/docview/1017977848
https://www.proquest.com/docview/884427486
Volume 155A
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