Article
Aniridia. A review.
Survey of ophthalmology - 1 Jan 2000
Nelson L B, Spaeth G L, Nowinski T S, Margo C E, Jackson L
Abstract excerpt
Aniridia occurs as a phenotypically heterogeneous condition which may be inherited as an autosomal dominant disorder or as part of several systemic syndromes. It has been linked with the loci of chromosomes 1 and 2 and associated with the deletion of the p-13 band of chromosome 11. Aniridia may occur in a highly penetrant form in association with other ocular abnormalities with poor vision or in a more variable...
Topics
- Cataract
- Chromosome Aberrations
- Chromosome Deletion
- Chromosome Disorders
- Chromosomes, Human, 6-12 and X
- Diagnosis, Differential
- Ectopia Lentis
- Genes, Dominant
- Glaucoma
- Humans
- Iris
- Kidney Neoplasms