Multicystic renal dysplasia (Q46441): Difference between revisions
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Displasia renal multicística, ou rim displásico multicístico (RDMC), é uma condição congênita em que um rim não se desenvolve adequadamente no útero, tornando-se uma coleção não funcional de cistos cheios de líquido em vez de tecido renal normal. Mais frequentemente afeta um único rim, permitindo que o outro rim saudável compense sua função, e geralmente é descoberta por meio de ultrassonografia pré-natal. A RDMC bilateral, que afeta ambos os rins, é uma condição muito grave com alto risco de insuficiência renal e frequentemente incompatível com a sobrevivência a longo prazo. | |||
| description / en | description / en | ||
Multicystic renal dysplasia, or multicystic dysplastic kidney (MCDK), is a congenital condition where a kidney fails to develop properly in the womb, becoming a non-functional collection of fluid-filled cysts instead of normal kidney tissue. It most often affects a single kidney, allowing the other healthy kidney to compensate for its function, and is usually discovered via prenatal ultrasound. Bilateral MCDK, affecting both kidneys, is a very serious condition with a high risk of kidney failure and is often incompatible with long-term survival. | |||
Revision as of 15:01, 13 August 2026
Multicystic renal dysplasia, or multicystic dysplastic kidney (MCDK), is a congenital condition where a kidney fails to develop properly in the womb, becoming a non-functional collection of fluid-filled cysts instead of normal kidney tissue. It most often affects a single kidney, allowing the other healthy kidney to compensate for its function, and is usually discovered via prenatal ultrasound. Bilateral MCDK, affecting both kidneys, is a very serious condition with a high risk of kidney failure and is often incompatible with long-term survival.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB30.9 |
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| English | Multicystic renal dysplasia |
Multicystic renal dysplasia, or multicystic dysplastic kidney (MCDK), is a congenital condition where a kidney fails to develop properly in the womb, becoming a non-functional collection of fluid-filled cysts instead of normal kidney tissue. It most often affects a single kidney, allowing the other healthy kidney to compensate for its function, and is usually discovered via prenatal ultrasound. Bilateral MCDK, affecting both kidneys, is a very serious condition with a high risk of kidney failure and is often incompatible with long-term survival. |
