Hip Dislocation, Congenital
"Hip Dislocation, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Congenital dislocation of the hip generally includes subluxation of the femoral head, acetabular dysplasia, and complete dislocation of the femoral head from the true acetabulum. This condition occurs in approximately 1 in 1000 live births and is more common in females than in males.
| Descriptor ID |
D006618
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| MeSH Number(s) |
C05.660.449 C16.131.621.449
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| Concept/Terms |
Hip Dislocation, Congenital- Hip Dislocation, Congenital
- Congenital Hip Dislocations
- Dislocations, Congenital Hip
- Hip Dislocations, Congenital
- Congenital Hip Dislocation
- Congenital Hip Displacement
- Congenital Hip Dysplasia
- Congenital Hip Dysplasias
- Dysplasias, Congenital Hip
- Hip Dysplasias, Congenital
- Hip, Dislocation Of, Congenital
- Dislocation, Congenital Hip
- Displacement, Congenital Hip
- Dysplasia, Congenital Hip
- Hip Displacement, Congenital
- Congenital Hip Displacements
- Displacements, Congenital Hip
- Hip Displacements, Congenital
- Hip Dysplasia, Congenital
- Congenital Dysplasia Of The Hip
- Dislocation Of Hip, Congenital
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Below are MeSH descriptors whose meaning is more general than "Hip Dislocation, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Hip Dislocation, Congenital".
This graph shows the total number of publications written about "Hip Dislocation, Congenital" by people in this website by year, and whether "Hip Dislocation, Congenital" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 1 | 0 | 1 |
| 2015 | 2 | 0 | 2 |
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Below are the most recent publications written about "Hip Dislocation, Congenital" by people in Profiles.
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Dikoglu E, Alfaiz A, Gorna M, Bertola D, Chae JH, Cho TJ, Derbent M, Alanay Y, Guran T, Kim OH, Llerenar JC, Yamamoto G, Superti-Furga G, Reymond A, Xenarios I, Stevenson B, Campos-Xavier B, Bonaf? L, Superti-Furga A, Unger S. Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome. Am J Med Genet A. 2015 Jul; 167(7):1501-9.
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Strauss KA, Jinks RN, Puffenberger EG, Venkatesh S, Singh K, Cheng I, Mikita N, Thilagavathi J, Lee J, Sarafianos S, Benkert A, Koehler A, Zhu A, Trovillion V, McGlincy M, Morlet T, Deardorff M, Innes AM, Prasad C, Chudley AE, Lee IN, Suzuki CK. CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease. Am J Hum Genet. 2015 Jan 08; 96(1):121-35.
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Rosen A, Gamble JG, Vallier H, Bloch D, Smith L, Rinsky LA. Analysis of radiographic measurements as prognostic indicators of treatment success in patients with developmental dysplasia of the hip. J Pediatr Orthop B. 1999 Apr; 8(2):118-21.