| Literature DB >> 2988231 |
Y Watanabe, T Todani, T Fujii, A Toki, S Uemura, Y Koike.
Abstract
A high incidence of congenital malformations with Wilms' tumor had been recognized lately. Aniridia, hemihypertrophy, chromosome deletion, urinary tract anomalies, and Wiedemann-Beckwith syndrome have often been observed in patients with Wilms' tumor. However, Wilms' tumor associated with Moyamoya disease, which refers to a stenosis of the distal portion of the carotid artery with an abnormal network in the brain base, has never been reported. In this report, a male child aged 28 mo. with Wilms' tumor associated with Moyamoya disease is presented.Entities:
Mesh:
Year: 1985 PMID: 2988231 DOI: 10.1055/s-2008-1059729
Source DB: PubMed Journal: Z Kinderchir ISSN: 0174-3082