Case Reports
Arthrogryposis multiplex congenita distal type II associated with facial abnormality, renal abnormality, Polydactyly and Hirschprung's disease
Authors:
S Sooriyabandara ,
Base Hospital, Mawanella, LK
APR Aluwihare
Department of surgery, Faculty of Medicine, University of Peradeniya, LK
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
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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