Multicystic renal dysplasia (Q46441): Difference between revisions

@@ description / pt-br / description / pt-br @@
+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.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1178642763
@@ Property / Canonical URI: https://id.who.int/icd/entity/1178642763 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LB30.9
@@ Property / CURIE: CID11:LB30.9 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LB30.9
@@ Property / Canary Token: dki-india-LB30.9 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+ICD Q257
@@ Property / Linked ICD 10: ICD Q257 / rank @@
+Normal rank

Latest 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
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.