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  2. 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 ]

  3. Cystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Cystic_kidney_disease

    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.

  4. Polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Polycystic_kidney_disease

    Polycystic kidney disease. Polycystic kidney disease (PKD or PCKD, also known as polycystic kidney syndrome) is a genetic disorder [ 5 ][ 6 ] in which the renal tubules become structurally abnormal, resulting in the development and growth of multiple cysts within the kidney. [ 7 ] These cysts may begin to develop in utero, in infancy, in ...

  5. Autosomal dominant polycystic kidney disease - Wikipedia

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

    Specialty. Medical genetics. Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common, life-threatening inherited human disorders and the most common hereditary kidney disease. [ 1 ][ 2 ] It is associated with large interfamilial and intrafamilial variability, which can be explained to a large extent by its genetic ...

  6. Potter sequence - Wikipedia

    en.wikipedia.org/wiki/Potter_sequence

    It can be caused by renal diseases such as bilateral renal agenesis (BRA), atresia of the ureter or urethra causing obstruction of the urinary tract, polycystic or multicystic kidney diseases, renal hypoplasia, amniotic rupture, toxemia, or uteroplacental insufficiency from maternal hypertension.

  7. Papillorenal syndrome - Wikipedia

    en.wikipedia.org/wiki/Papillorenal_syndrome

    Papillorenal syndrome is an autosomal dominant disorder that results from a mutation of one copy of the Pax2 gene, located on chromosome 10q24.3-q25.1. [2][11] The gene is important in the development of both the eye and the kidney. [citation needed] Autosomal dominant inheritance indicates that the gene responsible for the disorder is located ...

  8. Kidney disease - Wikipedia

    en.wikipedia.org/wiki/Kidney_disease

    The patient died with acute kidney injury. Kidney disease, or renal disease, technically referred to as nephropathy, is damage to or disease of a kidney. Nephritis is an inflammatory kidney disease and has several types according to the location of the inflammation. Inflammation can be diagnosed by blood tests.

  9. 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 ...

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