Article

Neonatal-Onset Glutaric Aciduria Type II: A Case Report and Literature Review

2026-06-30

Abstract excerpt

<title>Abstract</title> <p>Glutaric aciduria type II (GA2), also known as multiple acyl-CoA dehydrogenase deficiency (MADD), is a rare autosomal recessive disorder of fatty acid and amino acid metabolism with fewer than 100 neonatal-onset cases reported worldwide.[1] We report a term male neonate born to consanguineous parents (second-degree relatives) via in vitro fertilization who presented with sudden cardiore...

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Literature Corpus work: 5125d6a3-bf84-5834-9853-b0ac9bc09a9d
DOI: 10.21203/rs.3.rs-9638079/v1

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