 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
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| MeSH Number(s) |
C05.330.495 C05.660.585.512.380 C16.131.621.585.380
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| Concept/Terms |
Foot Deformities, Congenital- Foot Deformities, Congenital
- Congenital Foot Deformity
- Deformity, Congenital Foot
- Foot Deformity, Congenital
- Congenital Foot Deformities
- Deformities, Congenital Foot
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1983 | 0 | 1 | 1 | | 1989 | 0 | 1 | 1 | | 1993 | 1 | 0 | 1 | | 1995 | 1 | 0 | 1 | | 1997 | 0 | 1 | 1 | | 2000 | 1 | 1 | 2 | | 2004 | 1 | 0 | 1 | | 2006 | 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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Franke M, Ibrahim DM, Andrey G, Schwarzer W, Heinrich V, Schöpflin R, Kraft K, Kempfer R, Jerkovic I, Chan WL, Spielmann M, Timmermann B, Wittler L, Kurth I, Cambiaso P, Zuffardi O, Houge G, Lambie L, Brancati F, Pombo A, Vingron M, Spitz F, Mundlos S. Formation of new chromatin domains determines pathogenicity of genomic duplications. Nature. 2016 Oct 13; 538(7624):265-269.
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Dobbs MB, Gurnett CA, Pierce B, Exner GU, Robarge J, Morcuende JA, Cole WG, Templeton PA, Foster B, Bowcock AM. HOXD10 M319K mutation in a family with isolated congenital vertical talus. J Orthop Res. 2006 Mar; 24(3):448-53.
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Innis JW, Mortlock D, Chen Z, Ludwig M, Williams ME, Williams TM, Doyle CD, Shao Z, Glynn M, Mikulic D, Lehmann K, Mundlos S, Utsch B. Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model. Hum Mol Genet. 2004 Nov 15; 13(22):2841-51.
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Ruvinsky I, Chertkov O, Borue XV, Agulnik SI, Gibson-Brown JJ, Lyle SR, Silver LM. Genetics analysis of mouse mutations Abnormal feet and tail and rough coat, which cause developmental abnormalities and alopecia. Mamm Genome. 2002 Dec; 13(12):675-9.
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Goldberg MJ. Botulinum toxin type A improved ankle function in children with cerebral palsy and dynamic equinus foot deformity. J Bone Joint Surg Am. 2000 Jun; 82(6):874.
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Piersall LD, Dowton SB, McAlister WH, Waggoner DJ. Vertebral anomalies in a new family with ODED syndrome. Clin Genet. 2000 Jun; 57(6):444-8.
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Chitayat D, Grix A, Balfe JW, Abramowicz JS, Garza J, Fong CT, Silver MM, Saller DN, Bresnick GH, Giedion A, Lachman RS, Rimoin DL. Brachydactyly-short stature-hypertension (Bilginturan) syndrome: report on two families. Am J Med Genet. 1997 Dec 19; 73(3):279-85.
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Collins ED, Marsh JL, Vannier MW, Gilula LA. Spatial dysmorphology of the foot in Apert syndrome: three-dimensional computed tomography. Cleft Palate Craniofac J. 1995 May; 32(3):255-61; discussion 262.
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Craig CL, Goldberg MJ. Foot and leg problems. Pediatr Rev. 1993 Oct; 14(10):395-400.
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Verp MS. Urinary tract abnormalities in hand-foot-genital syndrome. Am J Med Genet. 1989 Apr; 32(4):555.
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