Bullous X linked retinoschisis: Clinical features and prognosis

British Journal of Ophthalmology

Volumn 102, Issue 5, 2018, Pages 622-624

  Hinds, Anne Marie ^a,b   Fahim, Abigail ^c   Moore, Anthony T ^a,b   Wong, Sui Chien ^a   Michaelides, Michel ^a,b  

^a MOORFIELDS EYE HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY OF MICHIGAN   (United States)

Author keywords

degeneration; dystrophy; genetics; retina

Indexed keywords

RETINOSCHISIN;

ADOLESCENT; ADULT; ARTICLE; BULLOUS X LINKED RETINOSCHISIS; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; FAMILY HISTORY; FOLLOW UP; GENE MUTATION; HEMIZYGOSITY; HUMAN; INFANT; NYSTAGMUS; ONSET AGE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGNOSIS; PUPIL DISEASE; REFRACTION ERROR; RETINA DETACHMENT; RETINOSCHISIS; RETROSPECTIVE STUDY; RS1 GENE; STRABISMUS; VISUAL ACUITY; VITREOUS FLOATERS; VITREOUS HEMORRHAGE; X CHROMOSOME LINKED DISORDER; COMPLICATION; CONGENITAL NYSTAGMUS; FEMALE; MALE; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; YOUNG ADULT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; INFANT; MALE; NYSTAGMUS, CONGENITAL; PROGNOSIS; RETINAL DETACHMENT; RETINOSCHISIS; RETROSPECTIVE STUDIES; STRABISMUS; VISUAL ACUITY; VITREOUS HEMORRHAGE; YOUNG ADULT;

EID: 85045780344     PISSN: 00071161     EISSN: 14682079     Source Type: Journal    
DOI: 10.1136/bjophthalmol-2017-310593     Document Type: Article

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