Late-onset multiple acyl-CoA dehydrogenase deficiency with breast cancer

Late-onset multiple acyl-CoA dehydrogenase deficiency with breast cancer

Abstract Background Multiple acyl-CoA dehydrogenase deficiency (MAAD) is a rare metabolic disorder resulting from an abnormality in fatty acid oxidation. There are three types of presentations: neonatal onset with or without congenital anomalies and the late-onset type. There is much clinical hetero...

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Bibliographic Details
Main Authors: Keechilat Pavithran, Divya Pachat, Dehannathparambil Kottarathil Vijaykumar
Format: Article
Language:English
Published: SpringerOpen 2020-12-01
Series:Egyptian Journal of Medical Human Genetics
Subjects:
Multiple acyl-CoA dehydrogenase deficiency
MADD
Glutaric aciduria type II
Fatty acid metabolism
Online Access:https://doi.org/10.1186/s43042-020-00121-0

Internet

https://doi.org/10.1186/s43042-020-00121-0

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