Collins–Pope syndrome
medical condition
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.
The public source identifies “Collins–Pope syndrome” as medical condition. This brief keeps that definition visible, then builds a research path around Collins, Pope and syndrome.
Why this record matters
A short description can identify a subject without explaining its stakes. For “Collins–Pope syndrome”, the useful work is to connect “medical condition” to the records capable of establishing context and consequence.
Named sources, stable identifiers and responsible institutions provide the strongest route from overview to verifiable evidence. The source revision retrieved here is dated Jul 17, 2025. The linked authority identifier is Q55783172. None of the 0 selected statements returned an explicit reference.
Overview language is designed for orientation and should not be treated as a substitute for the evidence cited beneath it. The lead is largely declarative, so disagreement and counter-evidence require a deliberate search beyond the opening account. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.
How to read it
Use the entry as an orientation point, then follow its citations and revision history. Names, dates and institutional relationships should be checked against the original record.
- Subject orientation
- Search vocabulary
- Locating named sources
The closest primary source, responsible institution and strongest cited specialist reference.
Three-step research path
- Establish the record: confirm the title “Collins–Pope syndrome”, its source revision and the description used here.
- Expand the search: follow Collins–Pope syndrome primary sources, Collins–Pope syndrome archive and Collins research across catalogues and specialist indexes.
- Test the account: compare the strongest cited source with the responsible institution’s current record and note any disagreement.
Questions for further research
- Which source most directly establishes the central claim about “Collins–Pope syndrome”?
- Which institution is responsible for the underlying evidence?
- What terminology or title could unlock a more precise catalogue search?
Search terms from this dossier
This entry incorporates text from “Collins–Pope syndrome” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.