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

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.
AuthorsS Manouvrier-Hanu, A C de la Chapelle, J P Farriaux
JournalPeĢdiatrie (Pediatrie) Vol. 43 Issue 4 Pg. 313-7 ( 1988) ISSN: 0031-4021 [Print] FRANCE
Vernacular TitleLe syndrome de Marden-Walker. Nouvelle observation et discussion de sa place dans les arthrogryposes.
PMID3047662 (Publication Type: Case Reports, English Abstract, Journal Article, Review)
Topics
  • Abnormalities, Multiple
  • Arthrogryposis (classification)
  • Female
  • Humans
  • Infant, Newborn

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