Two Cases of Oculofaciocardiodental (OFCD) Syndrome due to X-Linked BCOR Mutations Presenting with Infantile Hemangiomas: Phenotypic Overlap with PHACE Syndrome

BACKGROUND: Oculofaciocardiodental (OFCD) syndrome is due to mutations in BCOR (BCL-6 corepressor). OFCD has phenotypic overlaps with PHACE syndrome (Posterior fossa anomalies, Hemangioma, Arterial anomalies, Cardiac defects, Eye anomalies). Infantile hemangiomas are a key diagnostic criterion for P...

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Detalles Bibliográficos
Autores principales: Morgan, T. M., Colazo, J. M., Duncan, L., Hamid, R., Joos, K. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949664/
https://www.ncbi.nlm.nih.gov/pubmed/31956451
http://dx.doi.org/10.1155/2019/9382640

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949664/
https://www.ncbi.nlm.nih.gov/pubmed/31956451
http://dx.doi.org/10.1155/2019/9382640

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