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

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 myopathy, hype...

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Detalles Bibliográficos
Autores principales: Jacobi‐Polishook, Talia, Yosha‐Orpaz, Naama, Sagi, Yair, Lev, Dorit, Lerman‐Sagie, Tally
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653261/
https://www.ncbi.nlm.nih.gov/pubmed/33204590
http://dx.doi.org/10.1002/jmd2.12157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653261/
https://www.ncbi.nlm.nih.gov/pubmed/33204590
http://dx.doi.org/10.1002/jmd2.12157

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