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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...
Autores principales: | Jacobi‐Polishook, Talia, Yosha‐Orpaz, Naama, Sagi, Yair, Lev, Dorit, Lerman‐Sagie, Tally |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
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 |
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