enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Posterior urethral valve - Wikipedia

    en.wikipedia.org/wiki/Posterior_urethral_valve

    Posterior urethral valve (PUV) disorder is an obstructive developmental anomaly in the urethra and genitourinary system of male newborns. [1] A posterior urethral valve is an obstructing membrane in the posterior male urethra as a result of abnormal in utero development.

  3. Pyelectasis - Wikipedia

    en.wikipedia.org/wiki/Pyelectasis

    Pyelectasis is a dilation of the renal pelvis. It is a relatively common ultrasound finding in fetuses and is three times more common in male fetuses. In most cases pyelectasis resolves normally, having no ill effects on the baby. The significance of pyelectasis in fetuses is not clear.

  4. Bladder outlet obstruction - Wikipedia

    en.wikipedia.org/wiki/Bladder_outlet_obstruction

    Bladder outlet obstruction is included in the spectrum of congenital anomalies of the kidney and urinary tract (CAKUT). CAKUT is the most common cause of birth defects, occurring in 1 out of 1000 live births, and accounts for approximately half of all cases of chronic kidney disease and end-stage renal disease in children. [1] [2]

  5. Multicystic dysplastic kidney - Wikipedia

    en.wikipedia.org/wiki/Multicystic_dysplastic_kidney

    Multicystic dysplastic kidney (MCDK) is a condition that results from the malformation of the kidney during fetal development. The kidney consists of irregular cysts of varying sizes. Multicystic dysplastic kidney is a common type of renal cystic disease, and it is a cause of an abdominal mass in infants. [5]

  6. Duplicated ureter - Wikipedia

    en.wikipedia.org/wiki/Duplicated_ureter

    A hydronephrotic kidney may present as a palpable abdominal mass in the newborn, and may suggest an ectopic ureter or ureterocele. In older children, ureteral duplication may present as: [citation needed] Urinary tract infection – most commonly due to vesicoureteral reflux (flow of urine from the bladder into the ureter, rather than vice versa).

  7. Glomerulocystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Glomerulocystic_kidney_disease

    Glomerulocystic kidney disease can be inherited by autosomal dominant inheritance, develop due to urinary tract obstruction, [3] manifest in cell proliferation during organogenesis, [8] and develop through other related kidney diseases. Familial heritable GCKD can be inherited by offspring through adults which can cause GCKD in children or babies.

  8. Medullary sponge kidney - Wikipedia

    en.wikipedia.org/wiki/Medullary_sponge_kidney

    Medullary sponge kidney is a congenital disorder of the kidneys characterized by cystic dilatation of the collecting tubules in one or both kidneys. Individuals with medullary sponge kidney are at increased risk for kidney stones and urinary tract infection (UTI). Patients with MSK typically pass twice as many stones per year as do other stone ...

  9. Renal pelvis - Wikipedia

    en.wikipedia.org/wiki/Renal_pelvis

    [citation needed] A large "staghorn" kidney stone may block all or part of the renal pelvis. The size of the renal pelvis plays a major role in the grading of hydronephrosis . Normally, the anteroposterior diameter of the renal pelvis is less than 4 mm in fetuses up to 32 weeks of gestational age and 7 mm afterwards. [ 2 ]