Congenital Generalized Lipodystrophy Type 2 in a Patient From a High-Prevalence Area

Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disease characterized by the loss of body fat. The global prevalence of CGL is one in 10 million, and there are four subtypes. The case is presented of a 18-year-old woman from rural area of the north coast of Peru (Piura) with...

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Detalles Bibliográficos
Autores principales: Gonzalo, Miranda Manrique, Estefania, Chumbiauca Vela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686680/
https://www.ncbi.nlm.nih.gov/pubmed/29264552
http://dx.doi.org/10.1210/js.2017-00141

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686680/
https://www.ncbi.nlm.nih.gov/pubmed/29264552
http://dx.doi.org/10.1210/js.2017-00141

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