Clinical course in a patient with myopathic VLCAD deficiency during pregnancy with an affected baby

Very long‐chain acyl‐CoA dehydrogenase (VLCAD) deficiency is an autosomal recessive mitochondrial fatty acid oxidation disorder that manifests in three clinical forms: (a) severe, (b) milder, and (c) myopathic. Patients with the myopathic form present intermittent muscular symptoms such as myalgia,...

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Detalles Bibliográficos
Autores principales: Yamada, Kenji, Matsubara, Keiichi, Matsubara, Yuko, Watanabe, Asami, Kawakami, Sanae, Ochi, Fumihiro, Kuwabara, Kozue, Mushimoto, Yuichi, Kobayashi, Hironori, Hasegawa, Yuki, Fukuda, Seiji, Yamaguchi, Seiji, Taketani, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718132/
https://www.ncbi.nlm.nih.gov/pubmed/31497477
http://dx.doi.org/10.1002/jmd2.12061

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