Home > Health > Conditions and Diseases > Neurological Disorders > Chromosomal > WAGR Syndrome
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).
http://emedicine.medscape.com/article/989329-overview
Provides an overview of this unusual complex of congenital developmental abnormalities which include aniridia, genitourinary malformations and mental retardation.
http://ghr.nlm.nih.gov/condition/wilms-tumor-aniridia-genitourinary-anomalies-and-mental-retardation-syndrome
Provides information on this disorder and how it is inherited, with links to other resources.
http://www.genome.gov/26023527
Information on this rare genetic condition, its diagnosis, treatment and inheritance, provided by the National Human Genome Research Institute.
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=WAGR+Syndrome
Offers the synonyms, a general discussion and further resources.
http://www.wagr.org/
Information for families or physicians interested in learning more about WAGR Syndrome.
http://groups.yahoo.com/group/WAGR
A brief description of this support group. Join, post and read messages.
Home > Health > Conditions and Diseases > Neurological Disorders > Chromosomal > WAGR Syndrome
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