Successful pregnancy in a patient with mitochondrial cardiomyopathy due to ACAD9 deficiency

Abstract Acyl‐CoA dehydrogenase family member 9 (ACAD9) is an enzyme essential for the assembly of mitochondrial respiratory chain complex I. ACAD9 deficiency can cause lactic acidosis, myopathy, cardiomyopathy, intellectual disability, and early demise. We present a patient with mitochondrial myopa...

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Detalhes bibliográficos
Main Authors: Talia Jacobi‐Polishook, Naama Yosha‐Orpaz, Yair Sagi, Dorit Lev, Tally Lerman‐Sagie
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley 2020-11-01
Colecção:JIMD Reports
Assuntos:
ACAD9
cardiomyopathy
fatty acid oxidation
mitochondrial disease
pregnancy
riboflavin
Acesso em linha:https://doi.org/10.1002/jmd2.12157
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