Peters anomaly in PHACE syndrome
dc.contributor.author | Shabeeb, Nadine M. | |
dc.contributor.author | Plager, David A. | |
dc.contributor.author | Haggstrom, Anita N. | |
dc.contributor.department | Department of Dermatology, School of Medicine | en_US |
dc.date.accessioned | 2017-08-30T18:38:36Z | |
dc.date.available | 2017-08-30T18:38:36Z | |
dc.date.issued | 2017-08 | |
dc.description.abstract | 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. | en_US |
dc.eprint.version | Author's manuscript | en_US |
dc.identifier.citation | Shabeeb, N. M., Plager, D. A., & Haggstrom, A. N. (2017). Peters anomaly in PHACE syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. https://doi.org/10.1016/j.jaapos.2017.04.010 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/13983 | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.isversionof | 10.1016/j.jaapos.2017.04.010 | en_US |
dc.relation.journal | Journal of American Association for Pediatric Ophthalmology and Strabismus | en_US |
dc.rights | Publisher Policy | en_US |
dc.source | Author | en_US |
dc.subject | PHACE syndrome | en_US |
dc.subject | neurocutaneous disorder | en_US |
dc.subject | facial hemangioma | en_US |
dc.title | Peters anomaly in PHACE syndrome | en_US |
dc.type | Article | en_US |