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
in English
| 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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Arthrogryposis
/
Abnormalities, Multiple
/
Humans
/
Male
/
Infant, Newborn
Language:
English
Journal:
Ceylon Med J
Year:
2001
Type:
Article
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