Prader–Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion

We report a 17-year-old boy who met most of the major Prader−Willi syndrome (PWS) diagnostic criteria, including infantile hypotonia and poor feeding followed by hyperphagia, early-onset morbid obesity, delayed development, and characteristic facial features. However, unlike many children...

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Bibliographic Details
Main Authors: Qiming Tan, Kathryn J. Potter, Lisa Cole Burnett, Camila E. Orsso, Mark Inman, Davis C. Ryman, Andrea M. Haqq
Format: Article
Language:English
Published: MDPI AG 2020-01-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/11/2/128