Find Expert Doctors on Chromosome 11p Deletion Syndrome11 top medical experts on Chromosome 11p Deletion Syndrome across 3 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Chromosome 11p Deletion Syndrome: WAGR syndrome is a rare genetic syndrome in which there is a predisposition to several conditions, including certain malignancies, distinctive eye abnormalities, and/or intellectual disability .WAGR is an acronym for W ilms tumor , A niridia , G enitourinary problems (such as undescended testicles or hypospadias in males, or internal genital or urinary anomalies in females), and R ange of developmental delays .A combination of two or more of these conditions is usually present in most individuals with WAGR syndrome.The syndrome is caused by a deletion of genetic material on the short (p) arm of chromosome 11 .In most cases, this genetic change occurs spontaneously during early embryonic development (de novo) for unknown reasons (sporadic). Only rarely is the mutation inherited . Treatment of WAGR syndrome is aimed at addressing the specific symptoms that are present in each individual.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- Aniridia Foundation International (AFI)
PO Box 41
Manitowish Waters, WI 54545
Telephone: 901-409-1600
Website: https://www.make-a-miracle.org/
- International WAGR Syndrome Association
PO Box 2875
Montgomery Village, MD 20886
E-mail: ReachingOut@wagr.org
Website: http://www.wagr.org
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- Synonyms: 11p Deletion Syndrome
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