PHENOTYPIC HETEROGENEITY IN A FAMILY WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY WITH PREVENTION OF VISUAL LOSS IN AN AFFECTED MALE CHILD WITH LASER TREATMENT IN INFANCY.

Flores Pimentel, Mariana A; De la Huerta, Irina; Duncan, Jacque L; Slavotinek, Anne M; Moore, Anthony T; de Alba Campomanes, Alejandra G

Flores Pimentel, Mariana A; De la Huerta, Irina; Duncan, Jacque L; Slavotinek, Anne M; Moore, Anthony T; de Alba Campomanes, Alejandra G.

Affiliation

Flores Pimentel MA; Ophthalmology Department, University of California School of Medicine, San Francisco, Koret Vision Research Center, San Francisco, California.
De la Huerta I; Associated Retinal Consultants, William Beaumont Hospital, Royal Oak, Michigan; and.
Duncan JL; Ophthalmology Department, University of California School of Medicine, San Francisco, Koret Vision Research Center, San Francisco, California.
Slavotinek AM; Department of Pediatrics, Division of Genetics, University of San Francisco, San Francisco, California.
Moore AT; Ophthalmology Department, University of California School of Medicine, San Francisco, Koret Vision Research Center, San Francisco, California.
de Alba Campomanes AG; Ophthalmology Department, University of California School of Medicine, San Francisco, Koret Vision Research Center, San Francisco, California.

Retin Cases Brief Rep ; 15(3): 324-329, 2021 May 01.

Article in En | MEDLINE | ID: mdl-30074570

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinal Detachment / Retinal Hemorrhage / Blindness / Laser Coagulation / Eye Proteins / Familial Exudative Vitreoretinopathies / Nerve Tissue Proteins Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Adult / Child / Female / Humans / Infant / Male Language: En Journal: Retin Cases Brief Rep Year: 2021 Document type: Article Country of publication:

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