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 in | American journal of medical genetics. Part A Vol. 155A; no. 9; pp. 2112 - 2124 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.09.2011
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Online Access | Get full text |
ISSN | 1552-4825 1552-4833 1552-4833 |
DOI | 10.1002/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. |
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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. |
Author_xml | – sequence: 1 givenname: Margje surname: Sinnema fullname: Sinnema, Margje email: margje.sinnema@mumc.nl organization: Department of Clinical Genetics, Maastricht UMC, Maastricht University, Maastricht, The Netherlands – sequence: 2 givenname: Marian A. surname: Maaskant fullname: Maaskant, Marian A. organization: Governor Kremers Centre, Maastricht University, Maastricht, The Netherlands – sequence: 3 givenname: Henny M.J. surname: van Schrojenstein Lantman-de Valk fullname: van Schrojenstein Lantman-de Valk, Henny M.J. organization: Governor Kremers Centre, Maastricht University, Maastricht, The Netherlands – sequence: 4 givenname: I. surname: Caroline van Nieuwpoort fullname: Caroline van Nieuwpoort, I. organization: Department of Internal Medicine, Section of Endocrinology, VU University Medical Center and Neuroscience Campus Amsterdam, Amsterdam, The Netherlands – sequence: 5 givenname: Madeleine L. surname: Drent fullname: Drent, Madeleine L. organization: Department of Internal Medicine, Section of Endocrinology, VU University Medical Center and Neuroscience Campus Amsterdam, Amsterdam, The Netherlands – sequence: 6 givenname: Leopold M.G. surname: Curfs fullname: Curfs, Leopold M.G. organization: Department of Clinical Genetics, Maastricht UMC, Maastricht University, Maastricht, The Netherlands – sequence: 7 givenname: Constance T.R.M. surname: Schrander-Stumpel fullname: Schrander-Stumpel, Constance T.R.M. organization: Department of Clinical Genetics, Maastricht UMC, Maastricht University, Maastricht, The Netherlands |
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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 |
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Notes | istex:3665ABD06682EAF09ECCA8A300E71FEBD51FAABE ark:/67375/WNG-4TK5SJ8J-P ArticleID:AJMG34171 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. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
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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 e_1_2_7_5_1 e_1_2_7_3_1 e_1_2_7_9_1 e_1_2_7_7_1 e_1_2_7_19_1 e_1_2_7_17_1 e_1_2_7_41_1 e_1_2_7_13_1 e_1_2_7_43_1 e_1_2_7_11_1 e_1_2_7_45_1 e_1_2_7_47_1 e_1_2_7_26_1 e_1_2_7_49_1 Crino A (e_1_2_7_15_1) 2003; 162 e_1_2_7_28_1 e_1_2_7_50_1 e_1_2_7_25_1 e_1_2_7_23_1 e_1_2_7_33_1 e_1_2_7_54_1 e_1_2_7_21_1 e_1_2_7_35_1 e_1_2_7_56_1 e_1_2_7_37_1 e_1_2_7_39_1 Vogels A (e_1_2_7_52_1) 2004; 15 e_1_2_7_6_1 e_1_2_7_8_1 e_1_2_7_18_1 e_1_2_7_16_1 e_1_2_7_40_1 e_1_2_7_2_1 e_1_2_7_14_1 e_1_2_7_42_1 e_1_2_7_12_1 e_1_2_7_44_1 e_1_2_7_10_1 e_1_2_7_46_1 e_1_2_7_48_1 e_1_2_7_27_1 e_1_2_7_29_1 Kusuhara T (e_1_2_7_31_1) 1996; 36 Bhargava SA (e_1_2_7_4_1) 1996; 97 e_1_2_7_51_1 e_1_2_7_30_1 e_1_2_7_53_1 e_1_2_7_24_1 e_1_2_7_32_1 e_1_2_7_55_1 e_1_2_7_22_1 e_1_2_7_34_1 e_1_2_7_20_1 e_1_2_7_36_1 e_1_2_7_38_1 |
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. 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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 year: 2008 end-page: 351 article-title: Hormone‐dependent aging problems in women publication-title: Yonsei Med J – volume: 41 start-page: 789 year: 1999 end-page: 790 article-title: A woman with Prader–Willi syndrome gives birth to a healthy baby girl publication-title: Dev Med Child Neurol – volume: 90 start-page: 455 year: 2001 end-page: 459 article-title: Fertility in Prader–Willi syndrome: A case report with Angelman syndrome in the offspring publication-title: Acta Paediatr – volume: 16 start-page: 154 year: 2007 end-page: 156 article-title: Intellectual impairment and sexual health: Information needs publication-title: Br J Nurs – volume: 8 start-page: 1075 year: 2001 end-page: 1077 article-title: Rectal self‐mutilation, rectal bleeding and Prader–Willi syndrome publication-title: Arch Pediatr – volume: 91 start-page: 398 year: 1993 end-page: 402 article-title: Prader–Willi syndrome: Consensus diagnostic criteria publication-title: Pediatrics – volume: 342 start-page: 281 year: 1989 end-page: 285 article-title: Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader–Willi syndrome publication-title: Nature – volume: 304 start-page: 325 year: 1981 end-page: 329 article-title: Deletions of chromosome 15 as a cause of the Prader–Willi syndrome publication-title: N Engl J Med – volume: 103 start-page: 216 year: 2001 end-page: 222 article-title: Decreased bone mineral density in Prader–Willi syndrome: Comparison with obese subjects publication-title: Am J Med Genet – volume: 124A start-page: 158 year: 2004 end-page: 164 article-title: Unexpected death and critical illness in Prader–Willi syndrome: Report of ten individuals publication-title: Am J Med Genet Part A – volume: 56 start-page: 181 year: 1981 end-page: 186 article-title: Prader–Willi Syndrome after age 15 years publication-title: Arch Dis Child – volume: 10 start-page: 315 year: 2000 end-page: 319 article-title: Prevalence of symptomatic intracranial aneurysm and ischaemic stroke in pseudoxanthoma elasticum publication-title: Cerebrovasc Dis – volume: 9 start-page: 395 year: 1995 end-page: 400 article-title: Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15 publication-title: Nat Genet – volume: 29 start-page: 145 year: 1987 end-page: 152 article-title: Adults with Prader–Willi syndrome: A survey of 232 cases publication-title: Dev Med Child Neurol – volume: 356 start-page: 673 year: 2000 end-page: 675 article-title: Prader–Willi syndrome publication-title: Lancet – volume: 93 start-page: 4183 year: 2008 end-page: 4197 article-title: Recommendations for the diagnosis and management of Prader–Willi syndrome publication-title: J Clin Endocrinol Metab – volume: 12 start-page: 136 year: 2010 end-page: 151 article-title: Androgens and male aging: Current evidence of safety and efficacy publication-title: Asian J Androl – volume: 15 start-page: 12 year: 2004 end-page: 20 article-title: Prader–Willi syndrome: Advances in genetics, pathophysiology and treatment publication-title: Trends Endocrinol Metab – volume: 337 start-page: a2507 year: 2008 article-title: Managing health problems in people with intellectual disabilities publication-title: Br Med J – volume: 181 start-page: 452 year: 2009 end-page: 461 article-title: Cryptorchidism and testicular cancer: Separating fact from fiction publication-title: J Urol – volume: 96 start-page: 410 year: 2007 end-page: 413 article-title: Five‐years growth hormone (GH) treatment in adults with Prader–Willi syndrome publication-title: Acta Paediatr – volume: 63 start-page: 33 year: 2005 end-page: 39 article-title: Deaths in children with Prader–Willi syndrome. 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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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