Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Temporomandibular joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Cervical spine laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Lumbar spine laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Shoulder joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Elbow joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Wrist joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Hand joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Sacroiliac joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Hip joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Knee joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Ankle joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Foot joint laxity |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Hydrocephaly-tall stature-joint laxity syndrome is a multiple congenital anomalies syndrome described in two sisters and characterized by the presence of hydrocephalus (onset in infancy), tall stature, joint laxity, and thoracolumbar kyphosis. There have been no further descriptions in the literature since 1989. |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Dysmorphism-pectus carinatum-joint laxity syndrome is characterised by joint laxity, pectus carinatum and facial dysmorphism (mild frontal bossing, a beaked nose with a low nasal bridge, malar hypoplasia, chubby cheeks, a striking philtrum and arched upper lips). It has been described in two siblings. The mode of transmission is unknown. |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
dysplasie spondylo-épimétaphysaire avec hyperlaxité ligamentaire |
Is a |
False |
Joint laxity |
Inferred relationship |
Some |
|
De Barsy syndrome (DBS) is characterized by facial dysmorphism (down-slanting palpebral fissures, a broad flat nasal bridge and a small mouth) with a progeroid appearance, large and late-closing fontanel, cutis laxa (CL), joint hyperlaxity, athetoid movements and hyperreflexia, pre- and postnatal growth retardation, intellectual deficit and developmental delay, and corneal clouding and cataract. |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
Familial articular hypermobility syndrome (disorder) |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
A rare primary bone dysplasia with multiple joint dislocations characterized by stunted stature, articular hypermobility and spinal malalignment resulting in severe progressive kyphosis. Joint dislocations include bilateral dislocation of the radial heads with elbow contractures, feet (bilateral talipes equinovarus) and congenital dislocations of the hip and genu valgus. Joint laxity is particularly observed in fingers. Spinal changes include moderate platyspondyly with anterior projection of the vertebral bodies. Facial features of oval face with a flattened nasal bridge, button nose, long upper lip, prominent eyes and blue sclera are characteristic but variable. Patients may also present mild skin extensibility, spatulate terminal phalanges, lip and palate clefts, micrognathia and structural cardiac malformations. |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|
A rare primary bone dysplasia characterized by multiple joint dislocations, in particular in hips and knees present at birth, but the elbows, wrists, ankles, and patellae can also be affected; severe joint laxity, scoliosis, slender fingers with distal tapering, and growth deficiency developing in the post-natal period resulting in short stature. Gracile metacarpals and metatarsals, delayed bone age with poorly ossified carpal and tarsal bones, metaphyseal and epiphyseal dysplasia, slender ribs, and spondylar dysplasia are radiographical signs. Intelligence is usually normal. |
Is a |
True |
Joint laxity |
Inferred relationship |
Some |
|