ORPHA:2295
Familial articular hypermobility syndrome
Also called Familial joint instability syndrome, Familial joint laxity, Joint instability syndrome
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Adolescent, Childhood, Infancy
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:2295 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Joint hypermobility
- Congenital hip dislocation
- Patellar dislocation
- Abnormality of the knee
- Inguinal hernia
- Abnormality of femur morphology