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Article

Severe dietary protein sensitivity and hyperinsulinemic hypoglycemia in a patient with heterozygous mutation in HADH gene.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Sept 2010

Kaur S, Kulkarni K P, Kochar I P S

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Share to 3-Hydroxyacyl CoA Dehydrogenases
Share to Dietary Proteins
Share to Food Hypersensitivity
Share to Hyperinsulinism

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypoglycemia

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Source

Identifiers

PMID: 21175096
DOI: 10.1515/jpem.2010.152

Genes

HADH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Severe dietary protein sensitivity and hyperinsulinemic hypoglycemia in a patient with heterozygous mutation in HADH gene.PMID 21175096Read ↗

Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi family.Semantic proximity Read ↗

Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees.Semantic proximity Read ↗

Congenital hyperinsulinism due to mutations in HNF4A and HADH.Semantic proximity Read ↗

Novel insights into fatty acid oxidation, amino acid metabolism, and insulin secretion from studying patients with loss of function mutations in 3-hydroxyacyl-CoA dehydrogenase.Semantic proximity Read ↗

Evaluation of Body Composition and Biochemical Parameters in Adult PKUSemantic proximity Read ↗

Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase.Semantic proximity Read ↗

Familial hyperinsulinism caused by an activating glucokinase mutation.Semantic proximity Read ↗

Protein causes hyperinsulinemia: a Chinese patient with hyperinsulinism/hyperammonaemia syndrome due to a glutamate dehydrogenase gene mutation.Semantic proximity Read ↗

Protein-sensitive hypoglycemia without leucine sensitivity in hyperinsulinism caused by K(ATP) channel mutations.Semantic proximity Read ↗

A case of hyperinsulinism/hyperammonaemia syndrome: usefulness of the oral protein tolerance for the evaluation of treatment.Semantic proximity Read ↗

Identification of a diffuse form of hyperinsulinemic hypoglycemia by 18-fluoro-L-3,4 dihydroxyphenylalanine positron emission tomography/CT in a patient carrying a novel mutation of the HADH gene.Semantic proximity Read ↗

Two unrelated Chinese patients with hyperinsulinism /hyperammonemia (HI/HA) syndrome due to mutations in glutamate dehydrogenase gene.Semantic proximity Read ↗

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