1.
J Manipulative Physiol Ther
; 9(3): 213-7, 1986 Sep.
Article
in English
| MEDLINE
| ID: mdl-3772265
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.