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  2. Cystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Cystic_kidney_disease

    Cystic kidney disease refers to a wide range of hereditary, developmental, and acquired conditions [1] and with the inclusion of neoplasms with cystic changes, over 40 classifications and subtypes have been identified. Depending on the disease classification, the presentation may be at birth, or much later into adult life.

  3. 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]

  4. Polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Polycystic_kidney_disease

    Autosomal dominant polycystic kidney disease (ADPKD) is the most common of all the inherited cystic kidney diseases [12] [13] [14] with an incidence of 1:500 live births. [12] [14] Studies show that 10% of end-stage kidney disease (ESKD) patients being treated with dialysis in Europe and the U.S. were initially diagnosed and treated for ADPKD ...

  5. Congenital absence of the vas deferens - Wikipedia

    en.wikipedia.org/wiki/Congenital_absence_of_the...

    There are two main populations of CAVD; the larger group is associated with cystic fibrosis and occurs because of a mutation in the CFTR gene, [4] [5] while the smaller group (estimated between 10 and 40%) is associated with unilateral renal agenesis (URA). The mutational spectrum of CFTR in the first group differs from that observed in classic ...

  6. Renal agenesis - Wikipedia

    en.wikipedia.org/wiki/Renal_agenesis

    Renal agenesis is a medical condition in which one (unilateral) or both (bilateral) fetal kidneys fail to develop. Unilateral and bilateral renal agenesis in humans, mice and zebra fish has been linked to mutations in the gene GREB1L. [1] It has also been associated with mutations in the genes RET or UPK3A [2] in humans [3] and mice respectively.

  7. Medullary cystic kidney disease - Wikipedia

    en.wikipedia.org/.../Medullary_cystic_kidney_disease

    Medullary cystic kidney disease (MCKD) is an autosomal dominant kidney disorder characterized by tubulointerstitial sclerosis leading to end-stage renal disease.Because the presence of cysts is neither an early nor a typical diagnostic feature of the disease, and because at least four different gene mutations may give rise to the condition, the name autosomal dominant tubulointerstitial kidney ...

  8. Renal hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Renal_hypoplasia

    Segmental hypoplasia or Ask-Upmark kidney is a rare renal disease where a part of the kidney has undergone hypoplasia. The number of renal lobes is reduced, and the kidney size is less than two standard deviations from the average, with the weight often being over 50g in adults and 12–25g in children.

  9. Autosomal dominant polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Autosomal_dominant...

    Among American patients on the kidney-transplant waiting list (as of December 2011), 7256 (8.4%) were listed due to cystic kidney disease and of the 16,055 renal transplants performed in 2011, 2057 (12.8%) were done for patients with cystic kidney disease, with 1,189 from deceased donors and 868 from living donors. [80]

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