Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia

Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia

Congenital analbuminemia (CAA) is an inherited, autosomal recessive disorder with an incidence of 1:1,000,000 live birth. Affected individuals have a strongly decreased concentration, or complete absence, of serum albumin. The trait is usually detected by serum protein electrophoresis and immunochem...

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Bibliographic Details
Main Authors: Lorenzo Minchiotti, Gianluca Caridi, Monica Campagnoli, Francesca Lugani, Monica Galliano, Ulrich Kragh-Hansen
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-04-01
Series:Frontiers in Genetics
Subjects:
analbuminemia
autosomal recessive
frequency
preterm birth
hyperlipidemia
compensatory mechanisms
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2019.00336/full

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https://www.frontiersin.org/article/10.3389/fgene.2019.00336/full

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