Congenital generalized lipodystrophy in two siblings from Saudi Arabia: A case report

Congenital generalized lipodystrophy type 1 (CGL1) is a very rare autosomal recessive genetic mutation with generalized lipoatrophy and metabolic complications. We report CGL1 in two Saudi female siblings with lipoatrophy, diabetes mellitus, hypertriglyceridemia, steatohepatitis, and acanthosis due...

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Detalles Bibliográficos
Autores principales: Hummadi, Abdulrrahman, Nahari, Ahmed Ali, Alhagawy, Ali Jaber, Zakri, Ibrahim, Abutaleb, Raed, Yafei, Saeed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020436/
https://www.ncbi.nlm.nih.gov/pubmed/35474974
http://dx.doi.org/10.1002/ccr3.5720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020436/
https://www.ncbi.nlm.nih.gov/pubmed/35474974
http://dx.doi.org/10.1002/ccr3.5720

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