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Identification and Management of a Novel PRDM5 Gene Pathologic Variant in a Family With Brittle Cornea Syndrome.

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Bibliographic Details
Title:	Identification and Management of a Novel PRDM5 Gene Pathologic Variant in a Family With Brittle Cornea Syndrome.
Authors:	Sklar BA; Department of Ophthalmology, Wills Eye Hospital, Philadelphia PA., Pisuchpen P; Department of Ophthalmology, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand., Bareket M; Department of Ophthalmology, Kaplan Medical Center, Rehovot, Israel., Milman T; Eye Pathology Department, Wills Eye Hospital, Philadelphia PA., Eagle RC Jr; Eye Pathology Department, Wills Eye Hospital, Philadelphia PA., Minor J; Pediatric and Adult Strabismus Service, Wills Eye Hospital, Philadelphia PA., Procopio R; Ocular Genetics, Wills Eye Hospital, Philadelphia PA., Capasso J; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, Clinical Genetics, Golisano Children's Hospital, University of Rochester, Rochester, NY; and., Levin AV; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, Clinical Genetics, Golisano Children's Hospital, University of Rochester, Rochester, NY; and., Hammersmith K; Cornea Service, Wills Eye Hospital, Philadelphia PA.
Source:	Cornea [Cornea] 2023 Dec 01; Vol. 42 (12), pp. 1572-1577. Date of Electronic Publication: 2023 Sep 15.
Publication Type:	Case Reports; Journal Article
Journal Info:	Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8216186 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1536-4798 (Electronic) Linking ISSN: 02773740 NLM ISO Abbreviation: Cornea Subsets: MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1536-4798
DOI:	10.1097/ICO.0000000000003372