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What is Arthrogryposis?



What is Arthrogryposis?

  • Arthrogryposis: A rare congenital disorder characterized by reduced mobility of joints due to the build up of fibrous tissue in the joint.

Name and Aliases of Arthrogryposis

Main name of condition: Arthrogryposis

Other names or spellings for Arthrogryposis:

Guérin-Stern syndrome, Otto syndrome, Rocher-Sheldon syndrome, myodystrophy fetal deformans, amyoplasia congenita, AMC, arthrogryposis multiplex congenita, arthromyodysplasia, Congenital multiple arthrogryposis, Fibrous ankylosis of multiple joints, Arthrogryposis multiplex congenita (AMC), Rossi syndrome

Types of Arthrogryposis:

Subtypes of Arthrogryposis: Congenital multiple arthrogryposis
Parent types of Arthrogryposis: Rheumatic conditions

Organs Affected by Arthrogryposis:

joints

How serious is Arthrogryposis?

Complications of Arthrogryposis: see complications of Arthrogryposis

What causes Arthrogryposis?

Causes of Arthrogryposis: see causes of Arthrogryposis

How is it treated?

Treatments for Arthrogryposis: see treatments for Arthrogryposis


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