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Wilms tumor-aniridia syndrome

The Wilms tumor-aniridia syndrome was first described by Miller et al. who reported the common association of mental retardation, microcephaly, bilateral aniridia, Wilms tumor, and ambiguous genitalia in males. The occurrence of the syndrome is usually sporadic and has been found to be caused by an interstitial deletion of the short arm of chromosome 11.

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Protocol for the examination of specimens from patients with Wilms tumor (nephroblastoma) or other renal tumors of childhood
The College of American Pathologists offers these protocols to assist pathologists in providing clinically useful and relevant information when reporting ...
Diagnosis and referral of Wilms' Tumor
ABSTRACT Wilms' Tumor, also know as nephroblastoma, is a childhood renal tumor. The assessment and diagnosis of a Wilms' tumor is one of the many challenges ...

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