A Patient With PHACE Syndrome With Marked Ipsilateral Cerebral Atrophy
The association of posterior fossa malformation, facial cavernous hemangioma, arterial anomalies, coarctation of the aorta/cardiac defects and eye abnormalities (PHACE syndrome) represents a rare congenital anomaly with a broad spectrum of clinical manifestations and female predominance. We herein r...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2010-04-01
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Series: | Pediatrics and Neonatology |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S187595721060023X |