Subfoveal choroidal neovascularization in a 3-year-old child with North Carolina macular dystrophy

Journal of AAPOS

Volumn 11, Issue 6, 2007, Pages 614-615

  Rhee, David Y ^a   Reichel, Elias ^a   Rogers, Adam ^a   Strominger, Mitchell ^a  

^a NEW ENGLAND EYE CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILDHOOD DISEASE; CLINICAL FEATURE; FAMILY HISTORY; HUMAN; MALE; NORTH CAROLINA MACULAR DYSTROPHY; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; SUBRETINAL NEOVASCULARIZATION;

ATROPHY; CHILD, PRESCHOOL; CHOROID; CHOROIDAL NEOVASCULARIZATION; FOVEA CENTRALIS; HUMANS; MACULAR DEGENERATION; MALE; NORTH CAROLINA; PIGMENT EPITHELIUM OF EYE; RETINOSCOPY;

EID: 37049032334     PISSN: 10918531     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaapos.2007.06.010     Document Type: Article

References (7)

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3. Gass J.D.M. Stereoscopic Atlas of Macular Diseases: Diagnosis and Treatment. 3rd ed. (1987), C.V. Mosby Co, St. Louis (MO) 98-100
4. Small K.W. North Carolina macular dystrophy: Clinical features, genealogy, and genetic linkage analysis. Trans Am Ophthalmol Soc (1998) 925-961
5. Small K.W. North Carolina macular dystrophy. In: Traboulsi E.I. (Ed). Genetic Diseases of the Eye (1998), Oxford University Press, New York (NY) 367-371
6. Small K.W. North Carolina macular dystrophy is localized to 6q14-q16.2. (Abstract). Am J Hum Genet 51 Suppl (1992) A34
7. Small K.W., Hermsen V., Gurney N., Fetkenhour C.L., and Folk J.C. North Carolina macular dystrophy and central areolar pigment epithelial dystrophy: One family, one disease. Arch Ophthalmol 110 (1992) 515-518