Literature DB >> 17639594

Healthcare transition in persons with intellectual disabilities: general issues, the Maastricht model, and Prader-Willi syndrome.

Constance T R M Schrander-Stumpel1, Margje Sinnema, Lieke van den Hout, Marian A Maaskant, Henny M J van Schrojenstein Lantman-de Valk, Annemieke Wagemans, Jaap J P Schrander, Leopold M G Curfs.   

Abstract

In current healthcare, transitional healthcare is a very important and timely issue. Thanks to the major advances made in medical care and technology, many children with childhood onset diseases and/or genetic syndromes survive to adulthood. These children are at risk of not being provided with adequate healthcare as they reach adulthood. Healthcare transition is an essential part of healthcare provision, referred to as the shift from one type of healthcare to another. In Maastricht, we developed a transition/out clinic led by a medical doctor specialized in persons with intellectual disability (ID), together with a clinical geneticist. We aim to coordinate healthcare issues based on guidelines if available. Also questions concerning living, daily activities, relations, sexuality, and sterilization can be discussed. The aging process of persons with ID has been a topic of interest in recent years. Little is known about the aging process of people with specific syndromes, except for persons with Down syndrome. We present some data of a recent questionnaire study in persons with Prader-Willi syndrome. In only 50% in persons with a clinical diagnosis genetic test results could be reported. The majority of persons were obese. Diabetes mellitus, hypertension, skin problems, sleep apnea, and hormonal problems like osteoporosis and hypothyroidism were common. Psychiatric problems were frequent, especially in the persons with uniparental disomy. Osteoporosis and sleep apnoea seem to be underestimated. Further longitudinal research is necessary for a better understanding of the aging process in PWS. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17639594     DOI: 10.1002/ajmg.c.30136

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  8 in total

Review 1.  Developmentally appropriate healthcare for young people: a scoping study.

Authors:  Albert Farre; Victoria Wood; Tim Rapley; Jeremy R Parr; Debbie Reape; Janet E McDonagh
Journal:  Arch Dis Child       Date:  2014-09-26       Impact factor: 3.791

Review 2.  Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management.

Authors:  Angela E Lin; Craig T Basson; Elizabeth Goldmuntz; Pilar L Magoulas; Deborah A McDermott; Donna M McDonald-McGinn; Elspeth McPherson; Colleen A Morris; Jacqueline Noonan; Catherine Nowak; Mary Ella Pierpont; Reed E Pyeritz; Alan F Rope; Elaine Zackai; Barbara R Pober
Journal:  Genet Med       Date:  2008-07       Impact factor: 8.822

3.  Perceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome.

Authors:  D J Karas; G Costain; E W C Chow; A S Bassett
Journal:  J Intellect Disabil Res       Date:  2012-10-29

4.  Validation of an instrument to assess the delivery of patient-centred care to people with intellectual disabilities as perceived by professionals.

Authors:  Jane Murray Cramm; Anna Petra Nieboer
Journal:  BMC Health Serv Res       Date:  2017-07-11       Impact factor: 2.655

Review 5.  Healthcare Transition in Inherited Metabolic Disorders-Is a Collaborative Approach between US and European Centers Possible?

Authors:  Jessica I Gold; Karolina M Stepien
Journal:  J Clin Med       Date:  2022-09-30       Impact factor: 4.964

6.  An Adapted Model for Transition to Adult Care in Young Adults with Prader-Willi Syndrome.

Authors:  Maria Pedersen; Charlotte Höybye
Journal:  J Clin Med       Date:  2021-05-06       Impact factor: 4.241

7.  A population-based registry as a source of health indicators for rare diseases: the ten-year experience of the Veneto Region's rare diseases registry.

Authors:  Monica Mazzucato; Laura Visonà Dalla Pozza; Silvia Manea; Cinzia Minichiello; Paola Facchin
Journal:  Orphanet J Rare Dis       Date:  2014-03-19       Impact factor: 4.123

8.  Transition from childhood to adulthood in coeliac disease: the Prague consensus report.

Authors:  Jonas F Ludvigsson; Lars Agreus; Carolina Ciacci; Sheila E Crowe; Marilyn G Geller; Peter H R Green; Ivor Hill; A Pali Hungin; Sibylle Koletzko; Tunde Koltai; Knut E A Lundin; M Luisa Mearin; Joseph A Murray; Norelle Reilly; Marjorie M Walker; David S Sanders; Raanan Shamir; Riccardo Troncone; Steffen Husby
Journal:  Gut       Date:  2016-04-18       Impact factor: 23.059

  8 in total

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