Adult Prader-Willi Syndrome: An Update on Management

Author:

Ho-Ming Luk1

Affiliation:

1. Clinical Genetic Service, Department of Health, 3/F Cheung Sha Wan Jockey Club Clinic, 2 Kwong Lee Road, Shamshuipo, Kowloon, Hong Kong

Abstract

With the advancement of medical care, the survival of most patients with syndromal genetic disease is greatly improved. In this case report, we have reported an adult Prader-Willi syndrome patient who is being diagnosed at the age of 33. The clinical features and their associated complications during adulthood have been reviewed.

Publisher

Hindawi Limited

Subject

General Medicine

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Prader–Willi syndrome with atypical 15q deletion due to an unbalanced translocation between chromosomes 13 and 15;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2024-07-12

2. The use of the Montreal Cognitive Assessment (MoCA) to assess cognitive impairment in Prader-Willi syndrome;Advances in Mental Health and Intellectual Disabilities;2020-09-29

3. Expanded Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(14;15): Report and Review of the Literature;Cytogenetic and Genome Research;2019

4. Prader-Willi Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

5. Prader-Willi Syndrome;Atlas of Genetic Diagnosis and Counseling;2016

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