"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
|
| MeSH Number(s) |
C12.706.132 C12.777.829.132 C13.351.875.132 C13.351.968.829.132 C16.131.939.132
|
| 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 |
|---|
| 2008 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2014 | 2 | 0 | 2 |
| 2015 | 2 | 0 | 2 |
| 2017 | 1 | 0 | 1 |
| 2020 | 0 | 2 | 2 |
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Below are the most recent publications written about "Bladder Exstrophy" by people in Profiles.
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Fertility and sexuality issues in congenital lifelong urology patients: female aspects. World J Urol. 2021 Apr; 39(4):1021-1027.
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Recurrent constellations of embryonic malformations re-conceptualized as an overlapping group of disorders with shared pathogenesis. Am J Med Genet A. 2020 11; 182(11):2646-2661.
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ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development. Sci Rep. 2017 02 08; 7:42170.
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WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish. Hum Mol Genet. 2015 Sep 15; 24(18):5069-78.
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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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Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder. Hum Mol Genet. 2014 Oct 15; 23(20):5536-44.
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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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p63 (TP73L) a key player in embryonic urogenital development with significant dysregulation in human bladder exstrophy tissue. Int J Mol Med. 2010 Dec; 26(6):861-7.
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Cloacal exstrophy--pull-through or permanent stoma? A review of 53 patients. J Pediatr Surg. 2008 Jan; 43(1):164-8; discussion 168-70.
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Double discontinuous lipomyelomeningocele: CT findings. J Comput Assist Tomogr. 1985 May-Jun; 9(3):584-91.