Recurrent Hypoglycemia in a Case of Congenital Analbuminemia
Abstract
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 analbuminemia. We report the case of a female patient hospitalized for a streptococcal skin infection who showed recurrent hypoglycemia. A diagnosis...
Paper Details
Title
Recurrent Hypoglycemia in a Case of Congenital Analbuminemia
Published Date
Feb 25, 2020
Volume
2020
Pages
1 - 6
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