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

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

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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Bibliographische Detailangaben
Veröffentlicht in:Ceylon medical journal 2001-12, Vol.46 (4), p.156-157
Hauptverfasser: Sooriyabandara, S, Aluwihare, A P
Format: Artikel
Sprache:eng
Schlagworte:
Abnormalities, Multiple
Arthrogryposis - pathology
Humans
Infant, Newborn
Male
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Beschreibung
Zusammenfassung: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.
ISSN:0009-0875
2386-1274
DOI:10.4038/cmj.v46i4.6470