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PHACES syndrome--case report and literature review
Jelena Roganović1, Denise Adams
1Division of Hematology and Oncology, and Comprehensive Hemangiomas and Vascular Malformations Clinic, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA. jelena.roganovic@ri.t-com.hr
Abstract:
The case of a 2-month-old female infant with PHACES syndrome is reported. PHACES represents a broad spectrum of congenital anomalies, including the following primary features: posterior fossa brain malformations, large facial hemangiomas, arterial anomalies, cardiac defects and aortic coarctation, eye abnormalities, and ventral developmental defects. The literature on this rare condition is reviewed.
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