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

Authors:

S Sooriyabandara ,

Base Hospital, Mawanella, LK
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APR Aluwihare

Department of surgery, Faculty of Medicine, University of Peradeniya, LK
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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.

DOI: http://dx.doi.org/10.4038/cmj.v46i4.6470

Ceylon Medical Journal 2001; 46(4): 156-157

DOI: https://doi.org/10.4038/cmj.v46i4.6470
How to Cite: Sooriyabandara, S. and Aluwihare, A., 2014. Arthrogryposis multiplex congenita distal type II associated with facial abnormality, renal abnormality, Polydactyly and Hirschprung's disease. Ceylon Medical Journal, 46(4), pp.156–157. DOI: http://doi.org/10.4038/cmj.v46i4.6470
Published on 27 Jan 2014.
Peer Reviewed

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