Foot Deformities, Congenital
"Foot Deformities, 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.
Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth.
| Descriptor ID |
D005532
|
| MeSH Number(s) |
C05.330.495 C05.660.585.512.380 C16.131.621.585.512.500
|
| Concept/Terms |
Foot Deformities, Congenital- Foot Deformities, Congenital
- Congenital Foot Deformity
- Deformity, Congenital Foot
- Foot Deformity, Congenital
- Congenital Foot Deformities
- Deformities, Congenital Foot
|
Below are MeSH descriptors whose meaning is more general than "Foot Deformities, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Foot Deformities, Congenital".
This graph shows the total number of publications written about "Foot Deformities, Congenital" by people in this website by year, and whether "Foot Deformities, Congenital" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 0 | 1 | 1 |
| 2006 | 3 | 0 | 3 |
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Below are the most recent publications written about "Foot Deformities, Congenital" by people in Profiles.
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Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1. Am J Hum Genet. 2007 Jan; 80(1):105-11.
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Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region. Am J Med Genet A. 2006 Jul 01; 140(13):1384-95.
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Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis. Am J Med Genet A. 2006 Jul 01; 140(13):1440-6.
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Pediatric flatfoot: evaluation and management. J Am Acad Orthop Surg. 1999 Jan; 7(1):44-53.
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A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Am J Hum Genet. 1997 Mar; 60(3):555-64.