Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature

Moyamoya angiopathy (MA) is a rare cerebrovascular disorder characterised by the progressive occlusion of the internal carotid artery. Its aetiology is uncertain, but a genetic background seems likely, given the high MA familial rate. To investigate the aetiology of craniosynostosis and juvenile moy...

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Detalles Bibliográficos
Autores principales: Prontera, Paolo, Rogaia, Daniela, Mencarelli, Amedea, Ottaviani, Valentina, Sallicandro, Ester, Guercini, Giorgio, Esposito, Susanna, Bersano, Anna, Merla, Giuseppe, Stangoni, Gabriela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618647/
https://www.ncbi.nlm.nih.gov/pubmed/28926972
http://dx.doi.org/10.3390/ijms18091998

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618647/
https://www.ncbi.nlm.nih.gov/pubmed/28926972
http://dx.doi.org/10.3390/ijms18091998

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