Recurrent Hypoglycemia in a Case of Congenital Analbuminemia
Recurrent Hypoglycemia in a Case of Congenital Analbuminemia
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Publisher
Cairo, Egypt: Hindawi Publishing Corporation
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Language
English
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Publisher
Cairo, Egypt: Hindawi Publishing Corporation
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Contents
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 pati...
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Full title
Recurrent Hypoglycemia in a Case of Congenital Analbuminemia
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TN_cdi_doaj_primary_oai_doaj_org_article_d01e6a5779d54927a3a48c1f17a547be
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d01e6a5779d54927a3a48c1f17a547be
Other Identifiers
ISSN
2090-6501
E-ISSN
2090-651X
DOI
10.1155/2020/8452564
