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[Marden-Walker syndrome. New case and discussion about its role in arthrogryposes]
S Manouvrier-Hanu1, A C de la Chapelle, J P Farriaux
1Service de pédiatrie et génétique médicale, Hôpital Claude-Huriez, CHRU, Lille, France.
Pediatrie
|January 1, 1988
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.