Arthrogryposis Multiplex Congenita as Part of an Inherited Symptom Complex: Two Case Reports and a Review of the Literature
- 1 March 1978
- journal article
- review article
- Published by American Academy of Pediatrics (AAP) in Pediatrics
- Vol. 61 (3) , 417-422
- https://doi.org/10.1542/peds.61.3.417
Abstract
Two first cousins appear to have an autosomal recessive disorder consisting of arthrogryposis multiplex congenita (AMC), pterygium colli, congenital cervical spine fusions, and some features of the Eagle-Barrett syndrome. A review of the literature is summarized including the broad concepts of AMC as well as some syndromes in which AMC is but one manifestation.This publication has 4 references indexed in Scilit:
- Electromyographic and Histopathologic Correlations in ArthrogryposisArchives of Neurology, 1967
- MULTIPLE CONGENITAL CONTRACTURES - PUBLIC HEALTH CONSIDERATIONS OF ARTHROGRYPOSIS MULTIPLEX CONGENITA1963
- Arthrogryposis Multiplex CongenitaArchives of Neurology, 1961
- ARTHROGRYPOSIS MULTIPLEX DUE TO CONGENITAL MUSCULAR DYSTROPHYBrain, 1957