"Bladder Exstrophy" 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.
A birth defect in which the URINARY BLADDER is malformed and exposed, inside out, and protruded through the ABDOMINAL WALL. It is caused by closure defects involving the top front surface of the bladder, as well as the lower abdominal wall; SKIN; MUSCLES; and the pubic bone.
Descriptor ID |
D001746
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MeSH Number(s) |
C12.706.132 C12.777.829.132 C13.351.875.132 C13.351.968.829.132 C16.131.939.132
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Concept/Terms |
Bladder Exstrophy- Bladder Exstrophy
- Bladder Exstrophies
- Exstrophies, Bladder
- Exstrophy, Bladder
- Exstrophy Of Bladder
- Urinary Bladder Exstrophy
- Exstrophies, Urinary Bladder
- Exstrophy, Urinary Bladder
- Urinary Bladder Exstrophies
- Bladder Extrophy
- Bladder Extrophies
- Extrophies, Bladder
- Extrophy, Bladder
- Exstrophy of the Bladder
|
Below are MeSH descriptors whose meaning is more general than "Bladder Exstrophy".
Below are MeSH descriptors whose meaning is more specific than "Bladder Exstrophy".
This graph shows the total number of publications written about "Bladder Exstrophy" by people in this website by year, and whether "Bladder Exstrophy" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2006 | 2 | 0 | 2 |
2010 | 2 | 0 | 2 |
2013 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Bladder Exstrophy" by people in Profiles.
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Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation. Biomolecules. 2023 07 13; 13(7).
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A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. Commun Biol. 2022 Nov 09; 5(1):1203.
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Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy. PLoS Genet. 2015 Mar; 11(3):e1005024.
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Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region. Birth Defects Res A Clin Mol Teratol. 2014 Jun; 100(6):512-7.
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Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12. Birth Defects Res A Clin Mol Teratol. 2013 Mar; 97(3):133-9.
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Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. Birth Defects Res A Clin Mol Teratol. 2010 Sep; 88(9):757-61.
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Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy. Eur J Med Genet. 2010 Mar-Apr; 53(2):55-60.
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Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex. Am J Med Genet A. 2006 Nov 15; 140(22):2506-9.
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MTHFR 677 TT genotype in a mother and her child with Down syndrome, atrioventricular canal and exstrophy of the bladder: implications of a mutual genetic risk factor? Eur J Pediatr. 2006 Aug; 165(8):566-8.