 Congenital Abnormalities
"Congenital Abnormalities" 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.
Malformations of organs or body parts during development in utero.
| Descriptor ID |
D000013
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| MeSH Number(s) |
C16.131
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| Concept/Terms |
Congenital Abnormalities- Congenital Abnormalities
- Abnormality, Congenital
- Congenital Abnormality
- Deformities
- Deformity
- Congenital Defects
- Congenital Defect
- Defect, Congenital
- Defects, Congenital
- Abnormalities, Congenital
- Birth Defects
- Birth Defect
- Defect, Birth
- Defects, Birth
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Below are MeSH descriptors whose meaning is more general than "Congenital Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Congenital Abnormalities".
This graph shows the total number of publications written about "Congenital Abnormalities" by people in this website by year, and whether "Congenital Abnormalities" 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 |
|---|
| 1980 | 0 | 1 | 1 | | 1995 | 1 | 1 | 2 | | 2003 | 0 | 1 | 1 | | 2004 | 0 | 1 | 1 | | 2005 | 1 | 0 | 1 | | 2006 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 | | 2013 | 1 | 0 | 1 | | 2014 | 1 | 0 | 1 | | 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Congenital Abnormalities" by people in Profiles.
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Dimitriadis I, Pagidas K, Vaughan D, Kim YB. Mitotically Active Leiomyoma in a Woman with Mayer-Rokitansky-Küster-Hauser Syndrome: A Case Report. J Reprod Med. 2016 May-Jun; 61(5-6):299-301.
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San Agustin JT, Klena N, Granath K, Panigrahy A, Stewart E, Devine W, Strittmatter L, Jonassen JA, Liu X, Lo CW, Pazour GJ. Genetic link between renal birth defects and congenital heart disease. Nat Commun. 2016 Mar 22; 7:11103.
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Rao Damerla R, Gabriel GC, Li Y, Klena NT, Liu X, Chen Y, Cui C, Pazour GJ, Lo CW. Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models. Birth Defects Res C Embryo Today. 2014 Jun; 102(2):115-25.
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Ojha S, Ashland JE, Hersh C, Ramakrishna J, Maurer R, Hartnick CJ. Type 1 laryngeal cleft: a multidimensional management algorithm. JAMA Otolaryngol Head Neck Surg. 2014 Jan; 140(1):34-40.
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Mangones T, Visintainer P, Brumberg HL. Congenital anomalies, prematurity, and low birth weight rates in relation to nuclear power plant proximity1). J Perinat Med. 2013 Jul; 41(4):429-35.
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Phillips HM, Papoutsi T, Soenen H, Ybot-Gonzalez P, Henderson DJ, Chaudhry B. Neural crest cell survival is dependent on Rho kinase and is required for development of the mid face in mouse embryos. PLoS One. 2012; 7(5):e37685.
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Dueñas-García OF, Ramírez-Torres A, Diaz-Sotomayor M, Rico-Olvera H. [Perinatal outcomes of patients with gestational diabetes diagnosed by three different methods]. Ginecol Obstet Mex. 2011 Jul; 79(7):411-8.
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Dhomen N, Da Rocha Dias S, Hayward R, Ogilvie L, Hedley D, Delmas V, McCarthy A, Henderson D, Springer CJ, Pritchard C, Larue L, Marais R. Inducible expression of (V600E) Braf using tyrosinase-driven Cre recombinase results in embryonic lethality. Pigment Cell Melanoma Res. 2010 Feb; 23(1):112-20.
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Zhu H, Kartiko S, Finnell RH. Importance of gene-environment interactions in the etiology of selected birth defects. Clin Genet. 2009 May; 75(5):409-23.
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Kase JS, Visintainer P. The relationship between congenital malformations and preterm birth. J Perinat Med. 2007; 35(6):538-42.
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