Cakut

A range of renal and urinary tract malformations that vary from complete renal agenesis , to renal hypodysplasia, MULTICYSTIC DYSPLASTIC KIDNEY, duplex renal collecting system, ureteropelvic junction obstruction (UPJO), megaureter, posterior urethral valves (PUV), and vesicoureteral reflux (VUR). Up to 10% of cases are familial (autosomal dominant), although these are frequently asymptomatic or less severe; thus, PENETRANCE is incomplete. CAKUT occurs in 1 in 500 live births, and is lethal 1 in 2,000 births, it can also occur with other congenital anomalies, such as papillorenal syndrome (OMIM: 120330). OMIM: 610805

Also Known As:

Congenital Anomalies Of Kidney And Urinary Tract

Urogenital Diseases: 129
- Urologic Diseases: 817
  - Urinary Bladder Diseases: 180
    - Vesico-Ureteral Reflux: 1889
      - Cakut: 180
- Urogenital Abnormalities: 77
  - Cakut: 180
- Female Urogenital Diseases and Pregnancy Complications
  - Female Urogenital Diseases
    - Urologic Diseases: 817
      - Urinary Bladder Diseases: 180
        Vesico-Ureteral Reflux: 1889
        Cakut: 180
    - Urogenital Abnormalities: 77
      - Cakut: 180
- Male Urogenital Diseases
  - Urologic Diseases: 817
    - Urinary Bladder Diseases: 180
      - Vesico-Ureteral Reflux: 1889
        Cakut: 180
  - Urogenital Abnormalities: 77
    - Cakut: 180
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Urogenital Abnormalities: 77
    - Cakut: 180

Ruud R Bueters Selected Research

Ruud R Bueters Research Topics

Disease

Therapy/Procedure