 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 |
|---|
| 1982 | 0 | 1 | 1 | | 1983 | 1 | 1 | 2 | | 1984 | 0 | 1 | 1 | | 1985 | 0 | 1 | 1 | | 1989 | 1 | 0 | 1 | | 1990 | 1 | 0 | 1 | | 1991 | 2 | 0 | 2 | | 1992 | 0 | 2 | 2 | | 1993 | 1 | 2 | 3 | | 1994 | 1 | 0 | 1 | | 1995 | 1 | 0 | 1 | | 1996 | 2 | 1 | 3 | | 1998 | 0 | 1 | 1 | | 1999 | 1 | 4 | 5 | | 2000 | 0 | 1 | 1 | | 2001 | 0 | 1 | 1 | | 2002 | 1 | 0 | 1 | | 2003 | 2 | 1 | 3 | | 2004 | 0 | 1 | 1 | | 2005 | 1 | 1 | 2 | | 2006 | 1 | 0 | 1 | | 2008 | 3 | 1 | 4 | | 2009 | 1 | 1 | 2 | | 2010 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2012 | 0 | 1 | 1 | | 2013 | 0 | 1 | 1 | | 2014 | 1 | 2 | 3 | | 2016 | 0 | 1 | 1 | | 2017 | 1 | 1 | 2 | | 2018 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Congenital Abnormalities" by people in Profiles.
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Waggoner D, Wain KE, Dubuc AM, Conlin L, Hickey SE, Lamb AN, Martin CL, Morton CC, Rasmussen K, Schuette JL, Schwartz S, Miller DT. Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2018 10; 20(10):1105-1113.
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Antiel RM, Curlin FA, Lantos JD, Collura CA, Flake AW, Johnson MP, Rintoul NE, Brown SD, Feudtner C. Attitudes of paediatric and obstetric specialists towards prenatal surgery for lethal and non-lethal conditions. J Med Ethics. 2018 04; 44(4):234-238.
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Botros C, Iyer S, Tran AM, Goldberg RP. Vaginal vault prolapse in a patient with Mayer-Rokitansky-Küster-Hauser syndrome: a video case presentation. Int Urogynecol J. 2017 Nov; 28(11):1747-1749.
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Symmons O, Pan L, Remeseiro S, Aktas T, Klein F, Huber W, Spitz F. The Shh Topological Domain Facilitates the Action of Remote Enhancers by Reducing the Effects of Genomic Distances. Dev Cell. 2016 12 05; 39(5):529-543.
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Patel A, Costello JM, Backer CL, Pasquali SK, Hill KD, Wallace AS, Jacobs JP, Jacobs ML. Prevalence of Noncardiac and Genetic Abnormalities in Neonates Undergoing Cardiac Operations: Analysis of The Society of Thoracic Surgeons Congenital Heart Surgery Database. Ann Thorac Surg. 2016 Nov; 102(5):1607-1614.
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Hibbs SD, Bennett A, Castro Y, Rankin KM, Collins JW. Abdominal Wall Defects among Mexican American Infants: The Effect of Maternal Nativity. Ethn Dis. 2016 Apr 21; 26(2):165-70.
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Pandya KA, Koga H, Okawada M, Coran AG, Yamataka A, Teitelbaum DH. Vaginal anomalies and atresia associated with imperforate anus: diagnosis and surgical management. J Pediatr Surg. 2015 Mar; 50(3):431-7.
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Parravicini E, Lorenz JM. Neonatal outcomes of fetuses diagnosed with life-limiting conditions when individualized comfort measures are proposed. J Perinatol. 2014 Jun; 34(6):483-7.
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Rzhetsky A, Bagley SC, Wang K, Lyttle CS, Cook EH, Altman RB, Gibbons RD. Environmental and state-level regulatory factors affect the incidence of autism and intellectual disability. PLoS Comput Biol. 2014 Mar; 10(3):e1003518.
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Concepcion JP, Reh CS, Daniels M, Liu X, Paz VP, Ye H, Highland HM, Hanis CL, Greeley SA. Neonatal diabetes, gallbladder agenesis, duodenal atresia, and intestinal malrotation caused by a novel homozygous mutation in RFX6. Pediatr Diabetes. 2014 Feb; 15(1):67-72.
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