PMID: 3772265Sep 1, 1986Paper

The hand-foot-uterus syndrome: a case study

Journal of Manipulative and Physiological Therapeutics
G A LongmuirM Whitehead

Abstract

An autosomal dominant syndrome is described in 26 members of six generations in a single family. Distal extremity malformations are characteristic and superficially resemble those of arthrogryposis, chondroectodermal dysplasia, Cornelia de Lange syndrome, Faconi's anemia or Holt-Oram syndrome. There is an absence of spinal deformity, and females of the disorder have duplication of the genital tract.

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