Limb Deformities, Congenital
"Limb 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.
Congenital structural deformities of the upper and lower extremities collectively or unspecified.
| Descriptor ID |
D017880
|
| MeSH Number(s) |
C05.660.585 C16.131.621.585
|
| Concept/Terms |
Limb Deformities, Congenital- Limb Deformities, Congenital
- Congenital Limb Deformities
- Congenital Limb Deformity
- Deformities, Congenital Limb
- Deformity, Congenital Limb
- Limb Deformity, Congenital
|
Below are MeSH descriptors whose meaning is more general than "Limb Deformities, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Limb Deformities, Congenital".
This graph shows the total number of publications written about "Limb Deformities, Congenital" by people in this website by year, and whether "Limb 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 |
|---|
| 1996 | 1 | 0 | 1 |
| 1998 | 1 | 1 | 2 |
| 1999 | 1 | 1 | 2 |
| 2001 | 0 | 1 | 1 |
| 2003 | 1 | 1 | 2 |
| 2004 | 1 | 0 | 1 |
| 2005 | 1 | 3 | 4 |
| 2006 | 3 | 3 | 6 |
| 2008 | 2 | 0 | 2 |
| 2009 | 0 | 1 | 1 |
| 2010 | 1 | 2 | 3 |
| 2011 | 1 | 3 | 4 |
| 2012 | 1 | 2 | 3 |
| 2013 | 2 | 0 | 2 |
| 2014 | 1 | 1 | 2 |
| 2015 | 1 | 1 | 2 |
| 2016 | 2 | 0 | 2 |
| 2017 | 4 | 1 | 5 |
| 2018 | 1 | 0 | 1 |
| 2019 | 3 | 0 | 3 |
| 2020 | 6 | 1 | 7 |
| 2021 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Limb Deformities, Congenital" by people in Profiles.
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Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Hum Genet. 2024 Mar; 143(3):279-291.
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Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Hum Mutat. 2022 07; 43(7):900-918.
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Temporospatial regulation of intraflagellar transport is required for the endochondral ossification in mice. Dev Biol. 2022 02; 482:91-100.
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Birth defect co-occurrence patterns in the Texas Birth Defects Registry. Pediatr Res. 2022 04; 91(5):1278-1285.
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Robinow syndrome: Genital analysis, genetic heterogeneity, and associated psychological impact. Am J Med Genet A. 2021 12; 185(12):3601-3605.
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Craniofacial phenotypes associated with Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3606-3612.
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Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3593-3600.
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Extremity anomalies associated with Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3584-3592.
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Neurocognitive, adaptive, and psychosocial functioning in individuals with Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3576-3583.
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Characterization of the Robinow syndrome skeletal phenotype, bone micro-architecture, and genotype-phenotype correlations with the osteosclerotic form. Am J Med Genet A. 2020 11; 182(11):2632-2640.