Case Report: Successful Cerebral Revascularization and Cardiac Transplant in a 16-Year-Old Male With Syndromic BRCC3-Related Moyamoya Angiopathy

Background:BRCC3/MTCP1 deletions are associated with a rare familial moyamoya angiopathy with extracranial manifestations.Case: We report the case of an adolescent male presenting with progressive and symptomatic moyamoya angiopathy and severe dilated cardiomyopathy caused by a hemizygous deletion o...

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Bibliographic Details
Main Authors: Pierrick Pyra, Jean Darcourt, Marion Aubert-Mucca, Pierre Brandicourt, Olivier Patat, Emmanuel Cheuret, Karine Brochard, Annick Sevely, Lionel Calviere, Clément Karsenty
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Neurology
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Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2021.655303/full