Cloacal exstrophy (Q46445): Difference between revisions
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Malformação anorretal e geniturinária rara e complexa em que o reto, a vagina e o trato urinário compartilham um orifício evertido comum, acompanhado por uma onfalocele e um ânus imperfurado._x000D_ _x000D_ A extrofia da cloaca é uma malformação bem conhecida que inclui a persistência e a extrofia de uma cloaca que recebe ureteres, íleo e um intestino posterior rudimentar. A extrofia cloacal é um defeito congênito grave em que muitos dos órgãos abdominais (a bexiga e os intestinos) estão expostos. Freqüentemente causa a divisão dos órgãos genitais masculinos e femininos (especificamente, o pênis e o clitóris, respectivamente), e o ânus ocasionalmente é fechado. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Rare and complex anorectal and genitourinary malformation in which rectum, vagina and urinary tract share a common everted orifice, accompanied by an omphalocele and an imperforate anus. Exstrophy of the cloaca is a well-known malformation that includes the persistence and the exstrophy of a cloaca that receives ureters, ileum and a rudimentary hindgut. Cloacal exstrophy is a severe birth defect wherein much of the abdominal organs (the bladder and intestines) are exposed. It often causes the splitting of both male and female genitalia (specifically, the penis and clitoris respectively), and the anus is occasionally sealed. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/2004612103 / rank | |||||||||||||||
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CID11:LB17.3 | |||||||||||||||
| Property / CURIE: CID11:LB17.3 / rank | |||||||||||||||
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dki-india-LB17.3 | |||||||||||||||
| Property / Canary Token: dki-india-LB17.3 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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| Property / Linked ICD 10: ICD K254 / rank | |||||||||||||||
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Latest revision as of 15:02, 13 August 2026
Rare and complex anorectal and genitourinary malformation in which rectum, vagina and urinary tract share a common everted orifice, accompanied by an omphalocele and an imperforate anus. Exstrophy of the cloaca is a well-known malformation that includes the persistence and the exstrophy of a cloaca that receives ureters, ileum and a rudimentary hindgut. Cloacal exstrophy is a severe birth defect wherein much of the abdominal organs (the bladder and intestines) are exposed. It often causes the splitting of both male and female genitalia (specifically, the penis and clitoris respectively), and the anus is occasionally sealed.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB17.3 |
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| English | Cloacal exstrophy |
Rare and complex anorectal and genitourinary malformation in which rectum, vagina and urinary tract share a common everted orifice, accompanied by an omphalocele and an imperforate anus. Exstrophy of the cloaca is a well-known malformation that includes the persistence and the exstrophy of a cloaca that receives ureters, ileum and a rudimentary hindgut. Cloacal exstrophy is a severe birth defect wherein much of the abdominal organs (the bladder and intestines) are exposed. It often causes the splitting of both male and female genitalia (specifically, the penis and clitoris respectively), and the anus is occasionally sealed. |
Statements
CID11:LB17.3
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dki-india-LB17.3
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Concluído
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13 August 2026
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