| Collins–Pope syndrome | |
|---|---|
| Other names | Dislocation of the hip-dysmorphism syndrome |
 | |
| Specialty | Medical genetics |
| Symptoms | Congenital dislocation of the hip with facial dysmorphisms and joint hypermobility as the main characteristic of the syndrome. |
| Usual onset | Birth |
| Duration | Lifelong |
| Causes | Genetic mutation |
| Prevention | none |
| Prognosis | Good |
| Deaths | - |
Collins–Pope syndrome, also known as Dislocation of the hip-dysmorphism syndrome, is a rare autosomal dominant genetic disorder which is characterized by bilateral congenital hip dislocation, flattened mid-face, hypertelorism, epicanthus, puffy eyes, broad nasal bridge, carp-shaped mouth, and joint hypermobility. Additional findings include congenital heart defects, congenital knee dislocation, congenital inguinal hernia, and vesicoureteric reflux. It has been described in 4 members of a 2-generation family in the United Kingdom.