📂 Diseases
CAKUT2 — Definition
CAKUT2 / CAKUT2
CAKUT2 is a genetic subtype of congenital kidney and urinary tract anomalies (CHUT). This condition is characterized by congenital structural disorders of the kidneys and urinary tract. CAKUT2 syndrome can manifest itself in particular with findings such as renal agenesia, renal dysplasia or obstructive uropathy. Genetic mutations play an important role in the formation of these anomalies and the disease often manifests autozomal dominant inheritance.
Frequently Asked Questions
❓ What is CAKUT2?
CAKUT2; cAKUT2 is a genetic subtype of congenital kidney and urinary tract anomalies (CHUT). This condition is characterized by congenital structural disorders of the kidneys and urinary tract. CAKUT2 syndrome can manifest itself in particular with findings such as renal agenesia, renal dysplasia or obstructive uropathy. Genetic mutations play an important role in the formation of these anomalies and the disease often manifests autozomal dominant inheritance.
❓ What is CAKUT2 in Turkish?
The Turkish equivalent of "CAKUT2" is CAKUT2.
❓ Which medical field is CAKUT2 related to?
This term belongs to the Diseases category.