MeSH Browser

MeSH Supplementary: Hypoglycemia, leucine-induced
Unique ID: C537150
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537150
Entry Term(s): Leucine-sensitive hypoglycemia of infancy
Registry Numbers: 0
Heading Mapped to: Hypoglycemia / congenital
Frequency: 15
Note: A congenital metabolic disorder characterized by hypoglycemia following the consumption of LEUCINE-rich or high protein foods. It is caused by mutations in the SULFONYLUREA RECEPTORS (ABCC8) GENE. OMIM: 240800
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Hypoglycemia, leucine-induced MeSH Supplementary Concept Data 2024