ISSN: 1300-0365
Dil: Türkçe
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Aniridia-wilms Tumor Association (awta): A Case Report
Zühal SUYUGÜL*, Beyhan TÜYSÜZ**,Seher BAŞARAN***, Ayten ERGİNEL****, Asım CENANİ*****, Nezir SUYUGÜL******,*Uzm.Dr.İ.Ü. Cerrahpaşa Tıp Fak. Genetik ve Teratoloji Uygulama ve Araştırma Merkezi (GETAM) Göz Hast Kli.,**Yard.Doç.Dr. İ.Ü.Cerrahpaşa Tıp Fak. Çocuk Sağlığı ve Hastalıkları Genetik ve Teratoloji BD,***Doç.Dr. İ.Ü.Cerrahpaşa Tıp Fak. Pretam,****Prof.Dr.İ.Ü.Cerrahpaşa Tıp Fak Çocuk Sağlığı ve Hast. ABD,*****Prof.Dr. İ.Ü.Cerrahpaşa Tıp Fak Çocuk Sağlığı ve Hast.ABD, Genetik ve Teratoloji Uygulama Merkezi Müdürü,******Prof.Dr. İ.Ü.Cerrahpaşa Tıp Fak Göz Hast. ABD,İSTANBUL
ANIRIDIA-WILMS TUMOR ASSOCIATION (AWTA): A CASE REPORT
We analysed a patient genetically, who has aniridia associated with posterior polar cataract. Cystogenetic analysis
of mis patient revealed deletion at 11p12.1 (on chromosome 11's short arm (p) 12th band). Because of this region
deletions that lead to Wilms tumor, the patient was taken under our control. Indeed, she suffered from Wilms tumor
approximately 1 year later. Therefore, we described that the patient had aniridia-Wilms tumor association (AWTA). The
aniridia patients who are under the risk of Wilms tumor, must consult a genetic specialist.Keywords: Aniridia, Wilms tumor
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