Bilateral retinal involvement as a presenting sign of neurofibromatosis 2

Journal of Pediatric Ophthalmology and Strabismus

Volumn 39, Issue 1, 2002, Pages 49-51

  Önder, Feyza ^a   Cosar, C Banu ^a   Akbatur, Haluk ^a   Kural, Gülcan ^a  

^a NONE   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; BIOMICROSCOPY; CAFE AU LAIT SPOT; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; FLUORESCENCE ANGIOGRAPHY; HUMAN; MALE; NEUROFIBROMATOSIS; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; OPHTHALMOSCOPY; RETINA DISEASE; SKIN EXAMINATION; SLIT LAMP; VISION; VISUAL ACUITY;

EID: 0036179178     PISSN: 01913913     EISSN: None     Source Type: Journal    
DOI: 10.3928/0191-3913-20020101-12     Document Type: Article

References (13)

1. Clinical and genetic patterns of neurofibromatosis 1 and 2
2. Eye findings in bilateral acoustic (central) neurofibromatosis: Association with presenile lens opacities and cataracts but absence of Lisch in neurofibromatosis 2: Further significant correlations
3. Café-au-lait spots of the fundus in neurofibromatosis
4. Retinal hamartoma in neurofibromatosis 2
5. Bilateral retinal hamartomas in neurofibromatosis type 2
6. Combined hamartoma of the retina and retinal pigment epithelium in a patient with neurofibromatosis type 2
7. Blindness, deafness, quadriparesis, and a retinal malformation: The ravages of neurofibromatosis 2
8. Neurofibromatosis 2
9. Ocular findings associated with neurofibromatosis type 2
10. Ocular fundus in neurofibromatosis type 2
11. Ocular abnormalities in neurofibromatosis 2
12. Combined hamartomas of the retinal pigment epithelium and the retina
13. The ocular presentation of neurofibromatosis 2