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MON-103 Chromosome 15q13.3 Microdeletion And MAGEL2 Gene Mutation In A Pediatric Patient With Extreme Obesity And Tall Stature: A Case Report
Background: Clinical practice guidelines call for consideration of genetic syndromes in evaluation of pediatric patients with extreme early onset obesity with clinical features of genetic obesity syndromes or strong family history of obesity. We describe a case of two genetic variations discovered i...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Endocrine Society
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550931/ http://dx.doi.org/10.1210/js.2019-MON-103 |