Joint laxity, familial
MONDO:0007842A type of Ehlers-Danlos syndrome characterized by generalized joint hypermobility often complicated by dislocation of major joints, particularly the shoulder but in some cases the kneecap. Congenital hip dislocation has also been frequently reported. The syndrome has been described in several families. It is transmitted as an autosomal dominant trait, with high penetrance.
Also known as: EDS XI, Ehlers-Danlos syndrome type 11, formerly, Joint instability syndrome, familial joint instability syndrome, familial joint laxity, joint laxity, familial, EDS 11 (formerly), EDS Xi
14 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Hereditary disease
(172)
Syndromic disease
(24)
Ehlers-Danlos syndrome
(17)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)