Leucine-sensitive hypoglycemia of infancy

Leucine-sensitive hypoglycemia of infancy is a type of metabolic disorder.^[1] It is inherited in an autosomal dominant fashion.^[2] It is rare.^[3]

Names[edit | edit source]

Other names include hypoglycemia leucine-induced; hypoglycemia leucine induced; and familial infantile hypoglycemia precipitated by leucine.^[1]

References[edit | edit source]

↑ ^1.0 ^1.1 "Leucine-sensitive hypoglycemia of infancy | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 27 October 2019.
↑ "OMIM Entry - # 240800 - HYPOGLYCEMIA, LEUCINE-INDUCED; LIH". www.omim.org. Retrieved 27 October 2019.
↑ "Hypoglycemia, Leucine-Induced disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials". www.malacards.org. Retrieved 27 October 2019.

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[GARD2019-1] 1.0 ^1.1 "Leucine-sensitive hypoglycemia of infancy | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 27 October 2019.

[OMIM2019-2] "OMIM Entry - # 240800 - HYPOGLYCEMIA, LEUCINE-INDUCED; LIH". www.omim.org. Retrieved 27 October 2019.

[3] "Hypoglycemia, Leucine-Induced disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials". www.malacards.org. Retrieved 27 October 2019.

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