Arthrogryposis Multiplex CongenitaSymptoms, Doctors, Treatments, Advances & More
Arthrogryposis Multiplex Congenita Overview
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Learn About Arthrogryposis Multiplex Congenita
What is the definition of Arthrogryposis Multiplex Congenita?
Arthrogryposis multiplex congenita (AMC) refers to the development of multiple joint contractures affecting two or more areas of the body prior to birth. A contracture occurs when a joint becomes permanently fixed in a bent or straightened position, which can impact the function and range of motion of the joint and may lead to muscle atrophy. AMC is not a specific diagnosis, but rather a physical symptom that can be associated with many different medical conditions. It is suspected that AMC is related to decreased fetal movement during development which can have a variety of different causes, including environmental factors (i.e. maternal illness, limited space), single gene changes (autosomal dominant, autosomal recessive, X-linked), chromosomal abnormalities and various syndromes.
What are the alternative names for Arthrogryposis Multiplex Congenita?
- Arthrogryposis multiplex congenita
- Arthrogryposis
- Congenital arthromyodysplasia
- Congenital multiple arthrogryposis
- Fibrous ankylosis of multiple joints
- Guerin-Stern syndrome
- Guérin-Stern syndrome
- Myodystrophia fetalis deformans
- Otto syndrome
- Rocher-Sheldon syndrome
- Rossi syndrome
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Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center
What are the Latest Advances for Arthrogryposis Multiplex Congenita?
There is no recent research available for this condition. Please check back because thousands of new papers are published every week and we strive to find and display the most recent relevant research as soon as it is available.