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...

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Detalles Bibliográficos
Autores principales: Pyra, Pierrick, Darcourt, Jean, Aubert-Mucca, Marion, Brandicourt, Pierre, Patat, Olivier, Cheuret, Emmanuel, Brochard, Karine, Sevely, Annick, Calviere, Lionel, Karsenty, Clément
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044811/
https://www.ncbi.nlm.nih.gov/pubmed/33868155
http://dx.doi.org/10.3389/fneur.2021.655303

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