Molecular Biology of Wilm's Tumour
نویسندگان
چکیده
at an early age. Furthermore, a genetic predisposition to develop the tumour is associated with aniridia, genitourinary abnormalities and mental retardation (the WAGR syndrome) (1). Children with this rare syndrome typically carry a germline deletion involving band p13 on one of the two (parentally-derived) chromosome 11 homologues (2). The inherited 11 p deletion in WAGR and hereditary Wilms' patients is thought to represent the first of two events required for initiation of Wilms'
منابع مشابه
Successful treatment of intracaval and atrial extension of Wilms' tumour by chemotherapy.
A patient presenting with advanced Wilm's tumour was diagnosed as having inferior vena cava involvement with tumour thrombus extending up to the right atrium, and was treated with preoperative chemotherapy (vincristine, actinocymin D, epirubicin). Atrial and inferior vena cava thrombus disappeared and he underwent a successful nephrectomy.
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عنوان ژورنال:
دوره 102 شماره
صفحات -
تاریخ انتشار 1988