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.
MeSH Number(s)
C05.330.495
C05.660.585.512.380
C16.131.621.585.380
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 Harvard Catalyst Profiles by year, and whether "Foot Deformities, Congenital" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1993 | 0 | 1 | 1 |
| 1994 | 2 | 0 | 2 |
| 1995 | 2 | 0 | 2 |
| 1997 | 1 | 1 | 2 |
| 1998 | 0 | 1 | 1 |
| 1999 | 4 | 1 | 5 |
| 2000 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 1 | 0 | 1 |
| 2006 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 1 | 2 |
| 2011 | 2 | 2 | 4 |
| 2012 | 2 | 0 | 2 |
| 2013 | 2 | 0 | 2 |
| 2015 | 2 | 0 | 2 |
| 2016 | 1 | 0 | 1 |
| 2018 | 1 | 1 | 2 |
| 2019 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 2 | 0 | 2 |
Below are the most recent publications written about "Foot Deformities, Congenital" by people in Profiles.
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8 out of 10 patients do well after surgery for tarsal coalitions: A systematic review on 1284 coalitions. Foot Ankle Surg. 2022 Oct; 28(7):1110-1119.
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Oculodentodigital Dysplasia: A Cause of Hypomyelinating Leukodystrophy in Adults. Neurology. 2022 04 19; 98(16):675-677.
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Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder. Otol Neurotol. 2021 09 01; 42(8):e1143-e1151.
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Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study. Neurology. 2020 11 24; 95(21):e2866-e2879.
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Surgical Management of Complex Syndromic Craniosynostosis: Experience With a Rare Genetic Variant. J Craniofac Surg. 2020 Jan/Feb; 31(1):294-299.
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Rapidly Progressive Multisutural Craniosynostosis in a Patient With Jackson-Weiss Syndrome and a De Novo FGFR2 Pathogenic Variant. Cleft Palate Craniofac J. 2019 11; 56(10):1386-1392.
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Ankle and Foot Injuries in the Young Athlete. Semin Musculoskelet Radiol. 2018 Feb; 22(1):104-117.
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Polydactyly, postaxial, type B. Birth Defects Res. 2018 01; 110(2):134-141.
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A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016 Jun; 160(2):310-5.
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A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal. J Bone Miner Res. 2016 Apr; 31(4):882-9.