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Aniridia 1
- ... Absent iris Congenital aniridia Irideremia Genetic Testing Registry: Aniridia 1 Genetic Testing Registry: Congenital aniridia Isolated aniridia National ...
- Aniridia (American Association for Pediatric Ophthalmology and Strabismus)Eye Diseases/Specifics ... Eye Diseases ... American Association for Pediatric Ophthalmology and Strabismus ... GLOSSARY, TERMS, ACRONYMS, PHRASES, DEFINITIONS, DICTIONARY
- ... is estimated that one-third of people with aniridia actually have WAGR syndrome. Approximately 7 in 1,000 cases of Wilms tumor can be attributed ... in a series of 125 cases referred with aniridia. Am J Med Genet A. 2008 Mar 1;146A(5):558-69. doi: 10.1002/ajmg. ...
- ... in a series of 125 cases referred with aniridia. Am J Med Genet A. 2008 Mar 1;146A(5):558-69. doi: 10.1002/ajmg. ...
- Treatment Option Overview (Wilms Tumor and Other Childhood Kidney Tumors)
(National Cancer Institute)
Wilms Tumor/Treatments and Therapies ... Wilms Tumor ... Wilms tumor forms in the kidney in children and, rarely, adults. Learn about the risk factors and symptoms ... - Wilms Tumor/Start Here ... Wilms Tumor ... National Cancer Institute ... From the National Institutes of Health ... Wilms tumor forms in the kidney in children and, rarely, ...
- Wilms Tumor/Diagnosis and Tests ... Wilms Tumor ... National Cancer Institute ... From the National Institutes of Health ... Wilms tumor forms in the kidney in children and, ...
- Glaucoma in Children (American Association for Pediatric Ophthalmology and Strabismus)Glaucoma/Children ... Glaucoma ... American Association for Pediatric Ophthalmology and Strabismus ... GLOSSARY, TERMS, ACRONYMS, PHRASES, DEFINITIONS, DICTIONARY ... Shows ...
- ... known as Wilms tumor, an eye problem called aniridia, genitourinary anomalies, and a range of developmental delays. ... PAX6 gene disrupts normal eye development, leading to aniridia and other eye problems, and it may also ...
- ... Williamson KA, FitzPatrick DR. The genetic architecture of aniridia and Gillespie syndrome. Hum Genet. 2019 Sep;138( ...