Lower Extremity Deformities, Congenital
"Lower 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 LOWER EXTREMITY.
| Descriptor ID |
D038061
|
| MeSH Number(s) |
C05.660.585.512 C16.131.621.585.512
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Lower Extremity Deformities, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Lower Extremity Deformities, Congenital".
This graph shows the total number of publications written about "Lower Extremity Deformities, Congenital" by people in this website by year, and whether "Lower Extremity Deformities, Congenital" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2019 | 1 | 1 | 2 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Lower Extremity Deformities, Congenital" by people in Profiles.
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TBX5 variant with the novel phenotype of mixed-type total anomalous pulmonary venous return in Holt-Oram Syndrome and variable intrafamilial heart defects. Mol Med Rep. 2022 06; 25(6).
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Radial Ray Malformation. Am J Obstet Gynecol. 2019 12; 221(6):B16-B18.
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Pathogenic Variants in GPC4 Cause Keipert Syndrome. Am J Hum Genet. 2019 05 02; 104(5):914-924.
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An atypical case of Klippel-Tr?naunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report. BMC Pediatr. 2019 04 06; 19(1):95.
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TBX5: A Key Regulator of Heart Development. Curr Top Dev Biol. 2017; 122:195-221.
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Case Report: The Specter of Untreated Congenital Hypothyroidism in Immigrant Families. Pediatrics. 2016 05; 137(5).
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Syngnathia and obstructive apnea in a case of popliteal pterygium syndrome. Eur J Pediatr. 2014 Dec; 173(12):1741-4.
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Exome Sequencing Identifies DYNC1H1 Variant Associated With Vertebral Abnormality and Spinal Muscular Atrophy With Lower Extremity Predominance. Pediatr Neurol. 2015 Feb; 52(2):239-44.
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Antenatal diagnosis of camptomelic dysplasia. J Postgrad Med. 2006 Jan-Mar; 52(1):69-70.