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Medullary cystic kidney disease 2

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Medullary cystic kidney disease 2" returned 0 free, full-text review articles. First 0 results:
Medullary cystic kidney disease type 2.
Last Updated: Aug 15, 2019

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Medullary cystic kidney disease 2" returned 0 free, full-text editorial articles. First 0 results:
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Medullary cystic kidney disease 2" returned 2 free, full-text research articles. First 2 results:
A novel pattern of mutation in uromodulin disorders: autosomal dominant medullary cystic kidney disease type 2, familial juvenile hyperuricemic nephropathy, and autosomal dominant glomerulocystic kidney disease.
Last Updated: Aug 15, 2019

Autosomal dominant medullary cystic kidney disease type 2 (MCKD2), familial juvenile hyperuricemic nephropathy (FJHN), and autosomal dominant glomerulocystic kidney disease (GCKD) constitute a hereditary renal disease group that may lead to end-stage renal failure caused by mutations ...

Clinico-pathologic findings in medullary cystic kidney disease type 2.
Last Updated: Nov 13, 2018

Medullary cystic kidney disease type 2 is an uncommon autosomal dominant condition characterized by juvenile onset hyperuricemia, precocious gout and chronic renal failure progressing to end-stage renal disease in the 4th through 7th decades of life. A family suffering from this condition ...

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.
Last Updated: May 03, 2019

Medullary cystic kidney disease 2 (MCKD2) and familial juvenile hyperuricaemic nephropathy (FJHN) are both autosomal dominant renal diseases characterised by juvenile onset of hyperuricaemia, gout, and progressive renal failure. Clinical features of both conditions vary in presence ...

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