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Article

Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review.

World journal of pediatrics : WJP - 1 Aug 2016

Qian Gu-Ling, Hong Fang, Tong Fan, Fu Hai-Dong, Liu Ai-Min

Abstract excerpt

BACKGROUND: Glutaric acidemia type I (GA-I) is a rare metabolic disorder caused by mutation of the glutaryl- CoA dehydrogenase (GCDH) gene. The occurrence of rhabdomyolysis with GA-I is extremely rare. METHODS: We reported a child with recurrent rhabdomyolysis and undiagnosed glutaric acidemia type I (GA-I). And a literature review was performed. RESULTS: A 4.5-year-old girl was admitted to our hospital due to...

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Source

Identifiers

PMID: 27351573
DOI: 10.1007/s12519-016-0042-x

Genes

GCDH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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