Peters anomaly in PHACE syndrome

dc.contributor.authorShabeeb, Nadine M.
dc.contributor.authorPlager, David A.
dc.contributor.authorHaggstrom, Anita N.
dc.contributor.departmentDepartment of Dermatology, School of Medicineen_US
dc.date.accessioned2017-08-30T18:38:36Z
dc.date.available2017-08-30T18:38:36Z
dc.date.issued2017-08
dc.description.abstractPHACE 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.versionAuthor's manuscripten_US
dc.identifier.citationShabeeb, 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.2017.04.010en_US
dc.identifier.urihttps://hdl.handle.net/1805/13983
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.jaapos.2017.04.010en_US
dc.relation.journalJournal of American Association for Pediatric Ophthalmology and Strabismusen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectPHACE syndromeen_US
dc.subjectneurocutaneous disorderen_US
dc.subjectfacial hemangiomaen_US
dc.titlePeters anomaly in PHACE syndromeen_US
dc.typeArticleen_US
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