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
Wiley-Liss |
Subjects | |
Online Access | Get full text |
ISSN | 1552-4825 1552-4833 1552-4833 |
DOI | 10.1002/ajmg.a.34171 |
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Summary: | 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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Bibliography: | 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 |
ISSN: | 1552-4825 1552-4833 1552-4833 |
DOI: | 10.1002/ajmg.a.34171 |