[Marden-Walker syndrome. New case and discussion about its role in arthrogryposes]

Pediatrie. 1988;43(4):313-7.
[Article in French]

Abstract

A new case of Marden-Walker syndrome is reported. The Marden-Walker syndrome is a rare entity associating neonatal arthrogryposis and blepharophimosis with autosomal recessive inheritance. Its place among the various syndromes with neonatal arthrogryposis is discussed.

Publication types

  • Case Reports
  • English Abstract
  • Review

MeSH terms

  • Abnormalities, Multiple*
  • Arthrogryposis* / classification
  • Female
  • Humans
  • Infant, Newborn