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WAGR-syndrome

Deletions of llpl3 may result in Wilms tumor, aniridia, genitourinary malformations, and mental retardation (WAGR syndrome). In some patients, however, not all features are seen. Additionally, individual features of this syndrome may be inherited separately in a Mendelian fashion. Limited features may also be seen in patients without visible chromosomal deletions. The most likely mechanism for this finding is... [Pg.355]

A Wilms tumor can occur as part of complex disorder like the WAGR syndrome with Wilms tumor, aniridia, genital malformation and mental retardation. Responsible genes are in close vicinity on chromosome 11 in the region pl3 (WTl) and pl5.5 Mutation in the gene were found in... [Pg.77]

Syndromes WAGR Denys-Drash Frasier Beckwith- Perlman Wiedemann Simpson-Golabi-Behmel (type 1) Sotos Fanconi anemia D1 Mosaic variegated aneuploidy... [Pg.433]

See other pages where WAGR-syndrome is mentioned: [Pg.1859]    [Pg.139]    [Pg.134]    [Pg.1859]    [Pg.139]    [Pg.134]    [Pg.432]   
See also in sourсe #XX -- [ Pg.432 ]



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