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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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| izdano v: | Genes (Basel) |
|---|---|
| Main Authors: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
MDPI
2020
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| Teme: | |
| Online dostop: | 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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