Type IV 3-methylglutaconic (3-MGC) aciduria: A new case presenting with hepatic dysfunction

Efrat Broide*, Orly Elpeleg, Eli Lahat

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

We describe a new patient with type IV 3-methyl-glutaconic aciduria who presented with a clinical picture simulating a primary hepatic disorder subsequently followed with progressive neurologic impairment and an magnetic resonance imaging picture of Leigh syndrome.

Original languageEnglish
Pages (from-to)353-355
Number of pages3
JournalPediatric Neurology
Volume17
Issue number4
DOIs
StatePublished - Nov 1997

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