Polycystic Kidney, Autosomal Recessive
"Polycystic Kidney, Autosomal Recessive" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY.
Descriptor ID |
D017044
|
MeSH Number(s) |
C12.777.419.403.875.510 C13.351.968.419.403.875.510 C16.131.077.717.510 C16.320.798.510
|
Concept/Terms |
Polycystic Kidney, Autosomal Recessive- Polycystic Kidney, Autosomal Recessive
- Kidney, Polycystic, Autosomal Recessive
- Autosomal Recessive Polycystic Kidney Disease
- Polycystic Kidney and Hepatic Disease 1
- Polycystic Kidney Disease, Infantile, Type I
- Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive)
- Polycystic Kidney Disease, Autosomal Recessive
- Polycystic Kidney Disease, Infantile, Type 1
- Autosomal Recessive Polycystic Kidney
- ARPKD
|
Below are MeSH descriptors whose meaning is more general than "Polycystic Kidney, Autosomal Recessive".
- Diseases [C]
- Male Urogenital Diseases [C12]
- Urologic Diseases [C12.777]
- Kidney Diseases [C12.777.419]
- Kidney Diseases, Cystic [C12.777.419.403]
- Polycystic Kidney Diseases [C12.777.419.403.875]
- Polycystic Kidney, Autosomal Recessive [C12.777.419.403.875.510]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Female Urogenital Diseases [C13.351]
- Urologic Diseases [C13.351.968]
- Kidney Diseases [C13.351.968.419]
- Kidney Diseases, Cystic [C13.351.968.419.403]
- Polycystic Kidney Diseases [C13.351.968.419.403.875]
- Polycystic Kidney, Autosomal Recessive [C13.351.968.419.403.875.510]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
- Abnormalities, Multiple [C16.131.077]
- Polycystic Kidney Diseases [C16.131.077.717]
- Polycystic Kidney, Autosomal Recessive [C16.131.077.717.510]
- Genetic Diseases, Inborn [C16.320]
- Polycystic Kidney Diseases [C16.320.798]
- Polycystic Kidney, Autosomal Recessive [C16.320.798.510]
Below are MeSH descriptors whose meaning is more specific than "Polycystic Kidney, Autosomal Recessive".
This graph shows the total number of publications written about "Polycystic Kidney, Autosomal Recessive" by people in this website by year, and whether "Polycystic Kidney, Autosomal Recessive" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2005 | 1 | 0 | 1 |
2006 | 2 | 0 | 2 |
2008 | 1 | 0 | 1 |
2012 | 2 | 0 | 2 |
2014 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Polycystic Kidney, Autosomal Recessive" by people in Profiles.
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Maintenance Peritoneal Dialysis in Children With Autosomal Recessive Polycystic Kidney Disease: A Comparative Cohort Study of the International Pediatric Peritoneal Dialysis Network Registry. Am J Kidney Dis. 2020 03; 75(3):460-464.
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Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference. J Pediatr. 2014 Sep; 165(3):611-7.
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Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease. J Pediatr Gastroenterol Nutr. 2012 May; 54(5):580-7.
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More mud, less crystal? Ambivalence, disability, and PGD. Am J Bioeth. 2012; 12(4):26-8.
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A role for microRNA in cystic liver and kidney diseases. J Clin Invest. 2008 Nov; 118(11):3585-7.
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Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference. J Pediatr. 2006 Aug; 149(2):159-64.
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Predominant extrahepatic biliary disease in autosomal recessive polycystic kidney disease: a new association. Pediatr Transplant. 2006 May; 10(3):294-8.
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Liver disease in autosomal recessive polycystic kidney disease. Pediatr Transplant. 2005 Oct; 9(5):634-9.
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Congenital hypothyroidism in association with Caroli's disease and autosomal recessive polycystic kidney disease: patient report. J Pediatr Endocrinol Metab. 2005 Mar; 18(3):315-8.