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Autosomal Dominant Congenital Cataract Associated With Chromosomal Translocation [t(3;4)(p26.2;p15) ]
Paul D. Reese, MD;
Cathy M. Tuck-Muller, PhD;
Irene H. Maumenee, MD
Arch Ophthalmol. 1987;105(10):1382-1384.
Abstract
We studied a family in which congenital cataracts were found in a father and son who had a reciprocal translocation between the short arms of chromosomes 3 and 4 [t(3;4)(p26.2;p15) ]. The father's parents and brother had normal chromosomes and no evidence of cataracts. While results of these studies do not prove a causal relationship, they do strongly suggest that the areas near the break points involved in the translocation (3p26.2 and 4p15) would be good sites for further investigations into the genetic basis of this type of cataract.
Author Affiliations
From the Department of Ophthalmology, Tufts-New England Medical Center, Boston (Dr Reese); the Kennedy Institute and the Department of Pediatrics (Dr Tuck-Muller) and the Wilmer Ophthalmological Institute (Dr Maumenee), The Johns Hopkins University School of Medicine, Baltimore.
Footnotes
Accepted for publication June 15, 1987.
Reprint requests to Tufts-New England Medical Center, Department of Ophthalmology, 750 Washington St (Box 450), Boston, MA 02111 (Dr Reese).
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