Discordance of primary infantile glaucoma in monozygotic twins

American Journal of Ophthalmology

Volumn 128, Issue 1, 1999, Pages 97-98

  Zhang, Kang ^a   Jampel, Henry D ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL GLAUCOMA; DNA DETERMINATION; FEMALE; GENETIC ANALYSIS; HUMAN; PHENOTYPE; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; TWIN DISCORDANCE;

EID: 0033050829     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(99)00025-2     Document Type: Article

References (4)

1. Sarfarazi M., Akarsu A.N., Hossain A., et al. Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics. 30:1995;171-177.
2. Rasmussen D.H., Ellis P.P. Congenital glaucoma in identical twins. Arch Ophthalmol. 84:1970;827-830.
3. Fried K., Sachs R., Krakowsky D. Congenital glaucoma in only one of identical twins. Ophthalmologica. 174:1977;185-187.
4. Zhang K., Nguyen E., Crandall A., Donoso L.A. Genetic and molecular studies of macular dystrophies recent development . Surv Ophthalmol. 40:1995;51-61.