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Severe Early Onset Obesity due to a Novel Missense Mutation in Exon 3 of the Leptin Gene in an Infant from Northwest India
Monogenic obesity, caused by mutations in one of the genes involved in the control of hunger and satiety, is a rare cause of early onset obesity (EOO). The most common of the single gene alterations affect the leptin gene (LEP), resulting in congenital leptin deficiency that manifests as intense hyp...
Autores principales: | Dayal, Devi, Seetharaman, Keerthivasan, Panigrahi, Inusha, Muthuvel, Balasubramaniyan, Agarwal, Ashish |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083471/ https://www.ncbi.nlm.nih.gov/pubmed/29217499 http://dx.doi.org/10.4274/jcrpe.5501 |
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