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Arthrogryposis Multiplex Congenita: Neurogenic Type with Autosomal Recessive Inheritance
  1. A. Rosenmann,
  2. I. Arad
  1. Department of Human Genetics, Hadassah University Hospital, Jerusalem, Israel
  2. Department of Pediatrics, Hadassah University Hospital, Jerusalem, Israel


    An infant affected by severe arthrogryposis multiplex congenita leading to death in infancy due to neurogenic atrophy is described. Six other sibs were similarly affected. An autosomal recessive mode of inheritance is suggested.

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