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Arthrogryposis Multiplex Congenita: A Rare Case Report
Journal: International Journal of Science and Research (IJSR) (Vol.8, No. 3)Publication Date: 2019-03-05
Authors : Tejeshwari Gehlot; Yogesh Patel; Gunjan Kela;
Page : 849-853
Keywords : Arthrogryposis multiplex congenita; congenital syndrome; fetal akinesia;
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Abstract
Arthrogryposis Multiplex Congenita is a rare congenital syndrome characterized by multiple joint contractures. It is mainly due to fetal akinesia. Incidence is 1 in 3, 000 live births. It is associated with 300 different disorders. Management depends on the etiology, which makes the treatment different from one case to another. We study the case and followed up the child for prognosis and improvement.
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Last modified: 2021-06-28 17:30:42