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Published on: August 15, 2019
Evidence for inheritance in patients with VACTERL association
Benjamin D Solomon1, Daniel E Pineda-Alvarez, Manu S Raam
1Medical Genetics Branch, National Human Genome Research Institute, NIH MSC 3717, Bethesda, MD 20892, USA. solomonb@mail.nih.gov
None:
VACTERL/VATER association is typically a sporadic disorder. We present data on inheritance in 78 probands with VACTERL association, and show that 9% of probands have a primary relative with at least one component feature of VACTERL association. The prevalence of component features in first-degree relatives is significantly higher than expected in the general population, which has implications for counseling of affected families and for research into possible etiologies.
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