Collins–Pope syndrome, also known as Dislocation of the hip-dysmorphism syndrome,[1] 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.[2][3] Additional findings include congenital heart defects, congenital knee dislocation, congenital inguinal hernia, and vesicoureteric reflux.[4] It has been described in 4 members of a 2-generation family in the United Kingdom.[5][6]
| 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 | - |
References edit
- ^ Roberts, Sean (16 June 2022). "Collins Pope syndrome". NORD (National Organization for Rare Disorders). Retrieved 2022-07-12.
- ^ "Collins Pope syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022-07-12.
- ^ Bissonnette, Bruno; Luginbuehl, Igor; Marciniak, Bruno; Dalens, Bernard J. (2006), "Collins-Dennis-Clarke-Pope Syndrome", Syndromes: Rapid Recognition and Perioperative Implications, New York, NY: The McGraw-Hill Companies, retrieved 2022-07-12
- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Collins Pope syndrome". www.orpha.net. Retrieved 2022-07-12.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ Collins, A. L.; Dennis, N. R.; Clarke, N.; Pope, F. M. (1995-10-01). "A mother and three daughters with congenital dislocation of the hip and a characteristic facial appearance: a new syndrome?". Clinical Dysmorphology. 4 (4): 277–282. doi:10.1097/00019605-199510000-00001. ISSN 0962-8827. PMID 8574416. S2CID 28549863.
- ^ "Entry - 601450 - Dislocation of hip, congenital, with hyperextensibility of the fingers and facial dysmorphism - OMIM". omim.org. Retrieved 2022-07-12.
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