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 |
|---|
| 1995 | 1 | 0 | 1 |
| 2000 | 0 | 1 | 1 |
| 2005 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
| 2020 | 0 | 2 | 2 |
| 2023 | 1 | 0 | 1 |
| 2024 | 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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Blepharophimosis with intellectual disability and Helsmoortel-Van Der Aa Syndrome share episignature and phenotype. Am J Med Genet C Semin Med Genet. 2024 Dec; 196(4):e32089.
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Hashitoxicosis in a patient with Nicolaides-Baraitser Syndrome: a case report. Clin Dysmorphol. 2023 04 01; 32(2):77-79.
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Vertical transmission of a large calvarial ossification defect due to heterozygous variants of ALX4 and TWIST1. Am J Med Genet A. 2021 03; 185(3):916-922.
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De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome. Genet Med. 2020 11; 22(11):1838-1850.
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BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin-Siris and Nicolaides-Baraitser syndromes. Nat Commun. 2018 11 20; 9(1):4885.
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Prevalence and orthopedic management of foot and ankle deformities in Charcot-Marie-Tooth disease. Muscle Nerve. 2018 02; 57(2):255-259.
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Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability. Am J Med Genet A. 2017 Jan; 173(1):221-224.
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Fibular aplasia, tibial campomelia, and oligosyndactyly: a further patient with a 2-year follow-up. Clin Dysmorphol. 2014 Oct; 23(4):121-6.
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Bilateral os subtibiale and talocalcaneal coalitions in a college soccer player: a case report. J Foot Ankle Surg. 2011 Jul-Aug; 50(4):462-5.
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Terminal osseous dysplasia with pigmentary defects (TODPD): Follow-up of the first reported family, characterization of the radiological phenotype, and refinement of the linkage region. Am J Med Genet A. 2010 Jul; 152A(7):1825-31.