A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of Wilms' tumor (W), ANIRIDIA (A), genitourinary abnormalities (G), and mental retardation (R).
Related categories 2
eMedicine Pediatrics: WAGR Syndrome
Provides an overview of this unusual complex of congenital developmental abnormalities which include aniridia, genitourinary malformations and mental retardation.
Genetics Home Reference: WAGR Syndrome
Provides information on this disorder and how it is inherited, with links to other resources.
Learning about WAGR Syndrome
Information on this rare genetic condition, its diagnosis, treatment and inheritance, provided by the National Human Genome Research Institute.
NORD: WAGR Syndrome
Offers the synonyms, a general discussion and further resources.
Information for families or physicians interested in learning more about WAGR Syndrome.
Yahoo! Groups : WAGR Syndrome
A brief description of this support group. Join, post and read messages.
Last update:January 2, 2007 at 16:35:08 UTC