Wilms' Tumour
نویسندگان
چکیده
منابع مشابه
Hypoglycaemia with Wilms' Tumour.
Hypoglycaemia occurring in association with certain extrapancreatic tumours, mesodermal in type and mostly malignant, has become a well-established entity of organic hypoglycaemia. Conn and Seltzer (1955), in a review of spontaneous hypoglycaemia, added this group to the well-known causes of organic hypoglycaemia, namely, pancreatic, hepatic, anterior pituitary, adrenocortical and central nervo...
متن کاملAntenatally Diagnosed Wilms’ Tumour
Wilms' tumour (WT) is seldom seen in a neonate and prenatal diagnosis is rare. We present a case of antenatally diagnosed left sided WT with features of hydrops foetalis in a girl baby. Emergency LSCS was done at 34 weeks of gestation for foetal distress. Patient required mechanical ventilation for birth asphyxia and congestive cardiac failure. After stabilization, gross total resection of the ...
متن کاملPaternal occupation and Wilms' tumour in offspring.
A case-control study was conducted to test the hypothesis that paternal occupation is a risk factor for Wilms' tumour in offspring. Occupations associated with exposure to lead (Pb) and to hydrocarbons were examined by computing odds ratios, all of which were greater than unity but not by a statistically significant margin. When painters were considered separately, children whose fathers had be...
متن کاملRNA Processing: Wilms' tumour — the splicing connection?
Major isoforms of WT1--products of the tumour suppressor gene WT1, implicated in predisposition to Wilms' tumour--may preferentially interact with splicing factors, suggesting a role for WT1 in RNA processing.
متن کاملBeckwith–Wiedemann syndrome and Wilms’ tumour
Patients with rare overgrowth disorders, such as Beckwith–Wiedemann syndrome and Simpson–Golabi– Behmel syndrome, are predisposed to embryonal tumours, including Wilms’ tumour of the kidney. Therefore, these disorders offer a link between hyperplastic growth and cancer. Genetic lesions at chromosome 11p15 have been associated with Beckwith–Wiedemann syndrome and Wilms’ tumour for several years ...
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ژورنال
عنوان ژورنال: British Journal of Cancer
سال: 1976
ISSN: 0007-0920,1532-1827
DOI: 10.1038/bjc.1976.236