Arthrogryposis multiplex congenita distal type II associated with facial abnormality, renal abnormality, polydactyly and Hirschprung's disease.

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Date
2001-12-08
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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.
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The Ceylon Medical Journal.
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Citation
Sooriyabandara S, Aluwihare AP. Arthrogryposis multiplex congenita distal type II associated with facial abnormality, renal abnormality, polydactyly and Hirschprung's disease. The Ceylon Medical Journal. 2001 Dec; 46(4): 156-7
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https://imsear.searo.who.int/handle/123456789/48802
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Ceylon Medical Journal