North Carolina macular dystrophy: Clinicopathologic correlation

American Journal of Ophthalmology

Volumn 132, Issue 6, 2001, Pages 933-935

  Voo, Irene ^a   Glasgow, Ben J ^a   Flannery, John ^a   Udar, Nitin ^a   Small, Kent W ^a  

^a JULES STEIN EYE INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LIPOFUSCIN;

AGED; ARTICLE; BRUCH MEMBRANE; CASE REPORT; CHOROID CAPILLARY LAYER; CHOROID GYRATE ATROPHY; CLINICAL FEATURE; ELECTRORETINOGRAPHY; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MICROSCOPY; OPHTHALMOSCOPY; PHOTORECEPTOR CELL; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; SLIT LAMP; UNITED STATES;

EID: 0035205996     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(01)01184-9     Document Type: Article

References (5)

1. Small KW. North Carolina macular dystrophy: clinical features, genealogy, and genetic linkage analysis. Trans Am Ophthalmol Soc 1998:925-961.
2. Reichel MB, Kelsell RE, Fan J, et al. Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6q. Br J Ophthalmol 1998;82:1162-1168.
3. Pauleikhoff D, Sauer CG, Muller CR, et al. Clinical and genetic evidence for North Carolina macular dystrophy in a German family. Am J Ophthalmol 1997;124:412-415.
4. Spencer WH, editor. Ophthalmic pathology: an atlas and textbook, 4th ed., Vol. 2. Philadelphia: W.B. Saunders; 1996.
5. Dubovy SR, Hairston RJ, Schatz H, et al. Adult-onset foveomacular pigment epithelial dystrophy: clinicopathologic correlation of three cases. Retina 2000;20:638-649.