Upper Extremity Deformities, Congenital
"Upper Extremity 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 abnormalities of the UPPER EXTREMITY.
MeSH Number(s)
C05.660.585.988
C16.131.621.585.988
Below are MeSH descriptors whose meaning is more general than "Upper Extremity Deformities, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Upper Extremity Deformities, Congenital".
This graph shows the total number of publications written about "Upper Extremity Deformities, Congenital" by people in Harvard Catalyst Profiles by year, and whether "Upper Extremity 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 |
|---|
| 2002 | 1 | 0 | 1 |
| 2009 | 2 | 0 | 2 |
| 2011 | 1 | 1 | 2 |
| 2013 | 1 | 0 | 1 |
| 2016 | 2 | 0 | 2 |
| 2017 | 1 | 0 | 1 |
| 2018 | 0 | 2 | 2 |
| 2019 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
Below are the most recent publications written about "Upper Extremity Deformities, Congenital" by people in Profiles.
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Syndromic Involvement of Patients Presenting With Congenital Upper Limb Anomalies: An Analysis of 4,317 Cases. J Hand Surg Am. 2024 Apr; 49(4):311-320.
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Prenatal Diagnosis and Management of Thrombocytopenia-Absent Radius Syndrome. Neoreviews. 2022 06 01; 23(6):e429-e433.
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Congenital Upper Limb Differences Registry (CoULD): Registry Inclusion Effect. J Hand Surg Am. 2021 06; 46(6):515.e1-515.e11.
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Convergent Validity of PODCI and PROMIS Domains in Congenital Upper Limb Anomalies. J Hand Surg Am. 2020 Jan; 45(1):33-40.
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The Modified Vilkki Procedure: Vascularized Metatarsophalangeal Joint Transfer to Reconstruct a Full-Length Radius in Type III Radial Hypoplasia. J Hand Surg Am. 2020 Jan; 45(1):70.e1-70.e10.
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Thalidomide promotes degradation of SALL4, a transcription factor implicated in Duane Radial Ray syndrome. Elife. 2018 08 01; 7.
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Intraobserver and Interobserver Reliability of the Oberg-Manske-Tonkin (OMT) Classification: Establishing a Registry on Congenital Upper Limb Differences. J Pediatr Orthop. 2018 Jan; 38(1):69-74.
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Functional Impact of Congenital Hand Differences: Early Results From the Congenital Upper Limb Differences (CoULD) Registry. J Hand Surg Am. 2018 04; 43(4):321-330.
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Radial Longitudinal Deficiency: Recent Developments, Controversies, and an Evidence-Based Guide to Treatment. J Hand Surg Am. 2017 Jul; 42(7):546-563.
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KLF13 is a genetic modifier of the Holt-Oram syndrome gene TBX5. Hum Mol Genet. 2017 03 01; 26(5):942-954.