Hand Deformities, Congenital
"Hand 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 hand occurring at or before birth.
| Descriptor ID |
D006228
|
| MeSH Number(s) |
C05.390.408 C05.660.585.988.425 C16.131.621.585.988.500
|
| Concept/Terms |
Hand Deformities, Congenital- Hand Deformities, Congenital
- Congenital Hand Deformity
- Deformity, Congenital Hand
- Hand Deformity, Congenital
- Congenital Hand Deformities
- Deformities, Congenital Hand
|
Below are MeSH descriptors whose meaning is more general than "Hand Deformities, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Hand Deformities, Congenital".
This graph shows the total number of publications written about "Hand Deformities, Congenital" by people in this website by year, and whether "Hand 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 |
|---|
| 1995 | 2 | 0 | 2 |
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 1 | 2 |
| 2000 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2005 | 2 | 0 | 2 |
| 2007 | 1 | 0 | 1 |
| 2008 | 1 | 0 | 1 |
| 2010 | 1 | 2 | 3 |
| 2013 | 2 | 0 | 2 |
| 2014 | 2 | 0 | 2 |
| 2015 | 3 | 0 | 3 |
| 2016 | 1 | 2 | 3 |
| 2017 | 2 | 0 | 2 |
| 2018 | 0 | 2 | 2 |
| 2019 | 1 | 0 | 1 |
| 2020 | 4 | 1 | 5 |
| 2021 | 1 | 0 | 1 |
| 2022 | 2 | 1 | 3 |
| 2024 | 0 | 2 | 2 |
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Below are the most recent publications written about "Hand Deformities, Congenital" by people in Profiles.
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Congenital and Traumatic Conditions of the Pediatric Hand: Overview for the Radiologist. Semin Musculoskelet Radiol. 2024 Aug; 28(4):424-436.
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Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016-2023). Am J Med Genet A. 2024 Oct; 194(10):e63638.
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Recommending revised hepatoblastoma surveillance in children with a pathogenic ARID1A variant. Reply to "Cancer in ARID1A-Coffin-Siris syndrome: Review and report of a child with hepatoblastoma" by C?rcamo et al. 2022. Eur J Med Genet. 2023 02; 66(2):104694.
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Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic hernia. Am J Med Genet A. 2022 09; 188(9):2718-2723.
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Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects. Am J Med Genet A. 2022 05; 188(5):1384-1395.
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Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease-associated loci for BAFopathies. Genet Med. 2022 02; 24(2):364-373.
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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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A pilot clinical trial with losartan in Myhre syndrome. Am J Med Genet A. 2021 03; 185(3):702-709.
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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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"Coat Hanger" Appearance of the Ribs. N Engl J Med. 2020 Mar 26; 382(13):1257.