Bilateral macular holes: An unusual feature of Alport syndrome

Retina

Volumn 22, Issue 4, 2002, Pages 499-501

  Gupta, Viney ^a,b   Kumar, Neena ^a  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

^b Dev Eye Hospital   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALPORT SYNDROME; ARTICLE; CASE REPORT; CLINICAL FEATURE; HUMAN; MALE; RETINA DETACHMENT; RETINA MACULA HOLE; RETINOSCOPY; VISUAL IMPAIRMENT;

EID: 0036672019     PISSN: 0275004X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006982-200208000-00018     Document Type: Article

References (6)

1. Alport's syndrome: A genetic defect in biochemical composition of basement membrane of glomerulus, lens and inner ear
2. Clinical features and pathogenesis of Alport retinopathy
3. Autosomal recessive Alport syndrome: Linkage analysis and clinical features in two families
4. Identification of a distinct type 4 collagen α chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome
5. Ocular findings in 34 patients with Alport syndrome: Correlation of the findings to mutations in COL4A5 gene
6. Alport's syndrome with bilateral macular hole