Phenotypic Conservation in Patients With X-Linked Retinitis Pigmentosa Caused by RPGR Mutations

IMPORTANCE For patients with X-linked retinitis pigmentosa and clinicians alike, phenotypic variability can be challenging because it complicates counseling regarding patients’ likely visual prognosis. OBJECTIVE To evaluate the clinical findings from patients with X-linked retinitis pigmentosa with...

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Veröffentlicht in:	JAMA ophthalmology 2013-08, Vol.131 (8), p.1016-1025
Hauptverfasser:	Zahid, Sarwar, Khan, Naheed, Branham, Kari, Othman, Mohammad, Karoukis, Athanasios J, Sharma, Nisha, Moncrief, Ashley, Mahmood, Mahdi N, Sieving, Paul A, Swaroop, Anand, Heckenlively, John R, Jayasundera, Thiran
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Child Child, Preschool Electroretinography Eye Proteins - genetics Female Follow-Up Studies Genetic Diseases, X-Linked - diagnosis Genetic Diseases, X-Linked - genetics Humans Male Middle Aged Mutation - genetics Phenotype Retinitis Pigmentosa - diagnosis Retinitis Pigmentosa - genetics Retrospective Studies Visual Acuity - physiology Visual Fields - physiology Young Adult
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