PHACE syndrome is a rare neurocutaneous disorder, with a complex pathogenesis. It presents with a large facial hemangioma associated with anomalies of the posterior fossa of the brain, arterial anomalies, cardiac anomalies, coarctation of the aorta, and eye anomalies. Ocular abnormalities are rare. We report the first published case of an infant with PHACE syndrome and Peters anomaly
A case of Peters’ anomaly with bilateral crease on ear lobule and hypospadiuswas reported in a famil...
BACKGROUND AND PURPOSE: Head and neck infantile hemangiomas are common lesions that are rarely obser...
The acronym “PHACE” refers to the syndromic association of posterior fossa anomalies, hemangioma, ar...
The case of a 2-month-old female infant with PHACES syndrome is reported. PHACES represents a broad ...
Copyright © 2015 M. Fernández-Ibieta and J. C. López-Gutiérrez. This is an open access article di...
We report a case of a 29 day old infant who was referred for evaluation of a vision threatening exte...
Peters\u27 anomaly is a rare congenital eye condition characterized by anterior segment dysgenesis a...
Abstract: Infantile hemangioma can be linked to other organ malformations. In 1996, PHACE syndrome w...
Contains fulltext : 48785.pdf (publisher's version ) (Closed access)PHACES is an a...
Peter’s Anomaly, first described by Albert Peter in 1906, consists of a central corneal opacity rela...
Prior case reports have identified neurodevelopmental abnormalities in children with PHACE syndrome,...
Peters' anomaly is a rare congenital corneal opacity related to a malformation of the anterior segme...
PHACE association is a rare neurocutaneous condition in which facial hemangiomas associate with a sp...
Journal ArticleThe acronym PHACES describes a rare neurocutaneous syndrome that comprises posterior ...
Importance: A 2010 prospective study of 108 infants estimated the incidence of PHACE (posterior foss...
A case of Peters’ anomaly with bilateral crease on ear lobule and hypospadiuswas reported in a famil...
BACKGROUND AND PURPOSE: Head and neck infantile hemangiomas are common lesions that are rarely obser...
The acronym “PHACE” refers to the syndromic association of posterior fossa anomalies, hemangioma, ar...
The case of a 2-month-old female infant with PHACES syndrome is reported. PHACES represents a broad ...
Copyright © 2015 M. Fernández-Ibieta and J. C. López-Gutiérrez. This is an open access article di...
We report a case of a 29 day old infant who was referred for evaluation of a vision threatening exte...
Peters\u27 anomaly is a rare congenital eye condition characterized by anterior segment dysgenesis a...
Abstract: Infantile hemangioma can be linked to other organ malformations. In 1996, PHACE syndrome w...
Contains fulltext : 48785.pdf (publisher's version ) (Closed access)PHACES is an a...
Peter’s Anomaly, first described by Albert Peter in 1906, consists of a central corneal opacity rela...
Prior case reports have identified neurodevelopmental abnormalities in children with PHACE syndrome,...
Peters' anomaly is a rare congenital corneal opacity related to a malformation of the anterior segme...
PHACE association is a rare neurocutaneous condition in which facial hemangiomas associate with a sp...
Journal ArticleThe acronym PHACES describes a rare neurocutaneous syndrome that comprises posterior ...
Importance: A 2010 prospective study of 108 infants estimated the incidence of PHACE (posterior foss...
A case of Peters’ anomaly with bilateral crease on ear lobule and hypospadiuswas reported in a famil...
BACKGROUND AND PURPOSE: Head and neck infantile hemangiomas are common lesions that are rarely obser...
The acronym “PHACE” refers to the syndromic association of posterior fossa anomalies, hemangioma, ar...