Leucine-sensitive hypoglycemia of infancy is a type of metabolic disorder.
It is inherited in an
autosomal dominant
In genetics, dominance is the phenomenon of one variant (allele) of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome. The first variant is termed dominant and t ...
fashion.
It is rare.
Names
Other names include hypoglycemia leucine-induced; hypoglycemia leucine induced; and familial infantile hypoglycemia precipitated by leucine.
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References
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Metabolic disorders
Autosomal dominant disorders