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Arthrogryposis Multiplex Congenita: A Rare Case Report

Dr. Tejeshwari Gehlot, Dr. Yogesh Patel, Dr. Gunjan Kela

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.

Keywords: Arthrogryposis multiplex congenita, congenital syndrome, fetal akinesia,

Country: India, Subject Area: Pediatric Specialty

Pages: 849 - 853

Edition: Volume 8 Issue 3, March 2019

How to Cite this Article?

Dr. Tejeshwari Gehlot, Dr. Yogesh Patel, Dr. Gunjan Kela, "Arthrogryposis Multiplex Congenita: A Rare Case Report", International Journal of Science and Research (IJSR), https://www.ijsr.net/archive/v8i3/show_abstract.php?id=ART20196097, Volume 8 Issue 3, March 2019, 849 - 853

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