Bietti crystalline retinopathy affecting all 3 male siblings in a family

Archives of Ophthalmology

Volumn 118, Issue 1, 2000, Pages 129-131

  Chan, Wai Man ^b   Pang, Chi Pui ^b   Leung, Alfred T S ^b   Fan, Dorothy S P ^b   Cheng, Arthur C K ^b   Lam, Dennis S C ^a  

^a CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BIETTI CRYSTALLINE RETINOPATHY; CASE REPORT; CLINICAL FEATURE; CONTROLLED STUDY; EYE PHOTOGRAPHY; HUMAN; MALE; PRIORITY JOURNAL; RETINOPATHY; SIBLING;

ADULT; CRYSTALLIZATION; HUMANS; MALE; NUCLEAR FAMILY; PEDIGREE; RETINITIS PIGMENTOSA;

EID: 0033987463     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Bagolini B, Ioli-Spada G. Bieuttl's tapetoretinal degeneration with marginal corneal dystrophy. Am J. Ophtalmol. 1968;65:53-60.
2. Bernauer W. Daicker B. Biettl's corneal-retinal dystrophy a 16-year progression. Retina, 1992; 12:18-20.
3. Satalci AO, Yaman A, Berk AL, Sovley MF. Macular hold formation in Bietti's crystalline retinopathys a case report. Ophathalmol Genet. 1997;18: 139-141.
4. Richards BW, Brodsten DE. Nussbaum JS, Ferenez JR. Maeda K, Weiss L. Autosomal dominant crystalline dystrophy. Ophthalmology, 1991; 98:685-665.
5. Wilson Dj, Weleber RO, Klein ML, et al. Biettis crystalline dystrophy: a clinicopathologie correlative study. Arch Ophthalmol. 1989;107:213-221.
6. Bietti GB. Sualcune forme atipiche o rare di degenerazione retinicai degenerazione tappetoretiniche e quadri morbosi similari. Boll Oculist. 1937; 16:1159-1244.
7. Bietti GB. Ueber lamiliares Vorkominen von "Retinitis punctata albesceens" (verbunden mit "Dystropia marginalis cristallinca cornea"); Glitzen des Glaskorpers und anderen degenErativen Augenveranderungen. Klin Monatsbl AuGenheilkd. 1937;99:737-756.