Arthrogryposis multiplex congenita distal type II associated with facial abnormality, renal abnormality, polydactyly and Hirschprung's disease.
Ceylon Med J
;
2001 Dec; 46(4): 156-7
Article
Dans Anglais
| IMSEAR
| ID: sea-48802
ABSTRACT
A case of arthrogryposis multiplex congenita distal type II associated with facial abnormality, renal abnormality, postaxial poydactyly and Hirschprung's disease is described. It appears to be a new form of an autosomal recessive disorder.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Arthrogrypose
/
Malformations multiples
/
Humains
/
Mâle
/
Nouveau-né
langue:
Anglais
Texte intégral:
Ceylon Med J
Année:
2001
Type:
Article
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