Optical coherence tomography findings in foveal schisis

Archives of Ophthalmology

Volumn 122, Issue 7, 2004, Pages 1066-1067

  Greene, Joshua M ^a   Shakin, Eric P ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; DIAGNOSTIC VALUE; ELECTRORETINOGRAPHY; EYE PHOTOGRAPHY; HUMAN; MALE; NYSTAGMUS; OPTICAL COHERENCE TOMOGRAPHY; PRIORITY JOURNAL; RETINA FOVEA; RETINOSCHISIS; STRABISMUS; VISUAL ACUITY; X CHROMOSOME LINKED DISORDER; X CHROMOSOME RECESSIVE INHERITANCE; METHODOLOGY; PATHOLOGY; VISUAL SYSTEM EXAMINATION;

ADULT; DIAGNOSTIC TECHNIQUES, OPHTHALMOLOGICAL; FOVEA CENTRALIS; HUMANS; MALE; RETINOSCHISIS; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 3342912299     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.122.7.1066     Document Type: Article

References (4)

1. Condon GP, Brownstein S, Wang NS, Kearns JAF, Ewing CC. Congenital hereditary (juvenile X-linked) retinoschisis: histopachologic and ultrastructural findings in 3 eyes. Arch Ophthalmol. 1986;104:576-583.
2. Stanga PE, Chong NH, Reck AC, Hardcastle AJ, Holder GE. Optical coherence tomography and electrophysiology in X-linked juvenile retinoschisis associated with a novel mutation in the XLRS1 gene. Retina. 2001;21:78-80.
3. Manschot WA. Pathology of hereditary juvenile retinoschisis. Arch Ophthalmol. 1972;88: 131-138.
4. Menchini U, Brancato R, Virgili G, Pierro L. Unilateral macular retinoschisis with stellate foveal appearance in 2 females with myopia. Ophthalmic Surg Lasers. 2000;31:229-232.