"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 |
|---|
| 1996 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Foot Deformities, Congenital" by people in Profiles.
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Formation of new chromatin domains determines pathogenicity of genomic duplications. Nature. 2016 Oct 13; 538(7624):265-269.
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Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin-Siris and Nicolaides-Baraitser syndromes. Hum Genet. 2015 Jun; 134(6):553-68.
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A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling. Hum Mol Genet. 2013 Dec 20; 22(25):5121-35.
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Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome. Nat Genet. 2012 Feb 26; 44(4):445-9, S1.
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Genotype-phenotype correlation in eight new patients with a deletion encompassing 2q31.1. Am J Med Genet A. 2010 May; 152A(5):1213-24.
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Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndrome. Clin Genet. 1996 Feb; 49(2):98-102.
MeSH information
