Recurrent Hypoglycemia in a Case of Congenital Analbuminemia

In congenital analbuminemia (CAA), mutations in the albumin gene result in a severe deficiency or absence of plasma albumin. Only about 90 cases have been reported to date, but the specific features of glucose and lipid metabolism in congenital analbuminemia have only been studied in a rat model of...

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Detalles Bibliográficos
Autores principales: Litzel, Martin, Caridi, Gianluca, Lugani, Francesca, Campagnoli, Monica, Minchiotti, Lorenzo, Fischli, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063871/
https://www.ncbi.nlm.nih.gov/pubmed/32181025
http://dx.doi.org/10.1155/2020/8452564

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063871/
https://www.ncbi.nlm.nih.gov/pubmed/32181025
http://dx.doi.org/10.1155/2020/8452564

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