Molecular Evidence Of The Independent Origin Of Multiple Wilms Tumors In A Case Of WAGR Syndrome

UroToday.com - A study by Dr. Uccini, et al., evaluated the molecular evidence of the independent origin of multiple Wilms tumors in a patient who has WAGR syndrome. The paper was a description of the procedure, technique and its results. They had one

patient who was 1 year of age. that child developed two synchronous bilateral Wilms tumors that were resected by partial nephrectomy. Histologically, these tumors were fetal rhabdomyomatous nephroblastomas.

Original post by Women’s Health / Gynecology News From Medical News Today

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