| Literature DB >> 22422375 |
Alina Hilger1, Charlotte Schramm, Markus Draaken, Sadaf S Mughal, Gabriel Dworschak, Enrika Bartels, Per Hoffmann, Markus M Nöthen, Heiko Reutter, Michael Ludwig.
Abstract
The acronym VATER/VACTERL association is used to describe the non-random co-occurrence of vertebral defects (V), anorectal malformations (A), cardiac defects (C), tracheo-esophageal fistula with or without esophageal atresia (TE), renal malformations (R), and limb defects (L). We report a familial case of VATER/VACTERL association in which both the index case and her maternal uncle displayed four major component features of the disorder. A systematic literature search identified 12 previously described familial cases. However, on comparison, both members fulfilled the diagnostic criteria for VATER/VACTERL association only in one instance, and ours is the second such report. Although, a SNP array-based analysis identified no causal genomic alteration, the findings in the present family suggest that genetic factors are implicated in the development of the disorder.Entities:
Mesh:
Year: 2012 PMID: 22422375 DOI: 10.1007/s00383-012-3073-y
Source DB: PubMed Journal: Pediatr Surg Int ISSN: 0179-0358 Impact factor: 1.827