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 with PWS,...

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Detalles Bibliográficos
Publicado en:Genes (Basel)
Main Authors: Tan, Qiming, Potter, Kathryn J., Burnett, Lisa Cole, Orsso, Camila E., Inman, Mark, Ryman, Davis C., Haqq, Andrea M.
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2020
Assuntos:
Case Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7073628/
https://ncbi.nlm.nih.gov/pubmed/31991769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11020128
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