A Newborn with Athrogryposis Multiplex Congenital (AMC): A Case Report

Simon Pius *

Department of Paediatrics, University of Maiduguri Teaching Hospital, Maiduguri, Nigeria

Hauwa Yusuf Musa

Department of Paediatrics, University of Maiduguri Teaching Hospital, Maiduguri, Nigeria.

Yenti Machoko

Department of Paediatrics, University of Maiduguri Teaching Hospital, Maiduguri, Nigeria

Mustapha Bello

Department of Paediatrics, University of Maiduguri Teaching Hospital, Maiduguri, Nigeria

*Author to whom correspondence should be addressed.


Abstract

Arthrogryposis multiplex congenita (AMC) is constellation of contractions of multiple joints present at birth with fat or fibrous tissue partially or totally replacing muscles. Aetiological cause is from the interplay of genetic and environmental factors. It affects approximately 1 in 2-3000 live births. All four extremities are involved in50-60% of cases; lower limbs, in 30-40%, and upper limbs, in 10-15% of cases. Our patient is case of Amyoplasia with duodenal atresia. Had surgery and was seen in the clinic on follow up to 3 months. He has remain stable on physiotherapy.

Keywords: Arthrogryposis, muscle weaknessc, fibrosis, Amyoplasia, duodenal atresia


How to Cite

Pius, Simon, Hauwa Yusuf Musa, Yenti Machoko, and Mustapha Bello. 2018. “A Newborn With Athrogryposis Multiplex Congenital (AMC): A Case Report”. Asian Journal of Advanced Research and Reports 1 (1):1-6. https://doi.org/10.9734/ajarr/2018/v1i113010.