ICD·index Chapters ENESDE
LD26.41 category

Arthrogryposis multiplex congenita

Definition

Arthrogryposis multiplex congenita, comprises nonprogressive congenital conditions characterised by multiple joint contractures. The term is currently used in connection with a very heterogeneous group of disorders that all include multiple congenital joint contractures. The major cause of arthrogryposis is fetal akinesia due to fetal abnormalities (e.g. neurogenic, muscle, or connective tissue abnormalities; mechanical limitations to movement) or maternal disorders (e.g. infection, drugs, trauma, other maternal illnesses). Generalised fetal akinesia can also lead to polyhydramnios, pulmonary hypoplasia, micrognathia, ocular hypertelorism, and short umbilical cord. Lack of fetal movement causes extra connective tissue to develop around the joint, limiting movement and further aggravating the joint contracture.

Exclusions

Also indexed as

AMC - [arthrogryposis multiplex congenita]Arthrogryposis multiplex congenitaArthrogryposis multiplex congenita with whistling faceCrisponi syndromeMarden-Walker like syndromeMarden-Walker syndromeNeurogenic arthrogryposis multiplex congenitaVan den Ende-Gupta syndromeX-linked distal arthrogryposis multiplex congenitaamyoplasia congenitacongenital amyoplasiacongenital multiple arthrogryposiscongenital multiplex arthrogryposis

Nearby in Arthrogryposis syndromes