Literature DB >> 21456030

Wilms tumor in a patient with 22q11.2 microdeletion.

Paul T Finch1, Eniko K Pivnick, Wayne Furman, Christine C Odom.   

Abstract

22q11.2 deletion syndrome is the most common microdeletion syndrome. Wilms tumor is one of the most common solid tumors in childhood yet 22q11.2 deletion and Wilms tumor only once have been reported in the same patient. Here we describe a young patient with subtle clinical findings suggestive of 22q11.2 at the time of diagnosis who subsequently developed Wilms tumor. We assert the importance of a low threshold for screening for 22q11.2 deletion and the associated phenotypes and maintaining vigilance in screening for common primary malignancies in patients with known 22q11.2 deletion.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21456030     DOI: 10.1002/ajmg.a.33957

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

Review 1.  Genetics of pediatric renal tumors.

Authors:  Brigitte Royer-Pokora
Journal:  Pediatr Nephrol       Date:  2012-03-30       Impact factor: 3.714

2.  Risk of malignancy in 22q11.2 deletion syndrome.

Authors:  Toer Stevens; Jutte van der Werff Ten Bosch; Marjan De Rademaeker; Ann Van Den Bogaert; Machiel van den Akker
Journal:  Clin Case Rep       Date:  2017-03-02
  2 in total

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