Adult Prader-Willi Syndrome: An Update on Management
Author:
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
Publisher
Hindawi Limited
Subject
General Medicine
Link
http://downloads.hindawi.com/journals/crig/2016/5251912.pdf
Reference6 articles.
1. Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders
2. A long-term population-based clinical and morbidity review of Prader-Willi syndrome in Western Australia
3. Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region
4. Death in adults with Prader-Willi syndrome may be correlated with maternal uniparental disomy
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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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