 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
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| 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
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| 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
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 0 | 1 | 1 | | 2008 | 1 | 0 | 1 | | 2010 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Polycystic Kidney, Autosomal Recessive" by people in Profiles.
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Olson RJ, Hopp K, Wells H, Smith JM, Furtado J, Constans MM, Escobar DL, Geurts AM, Torres VE, Harris PC. Synergistic Genetic Interactions between Pkhd1 and Pkd1 Result in an ARPKD-Like Phenotype in Murine Models. J Am Soc Nephrol. 2019 11; 30(11):2113-2127.
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Jiang L, Fang P, Septer S, Apte U, Pritchard MT. Inhibition of Mast Cell Degranulation With Cromolyn Sodium Exhibits Organ-Specific Effects in Polycystic Kidney (PCK) Rats. Int J Toxicol. 2018 Jul/Aug; 37(4):308-326.
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Holditch SJ, Schreiber CA, Harris PC, LaRusso NF, Ramirez-Alvarado M, Cataliotti A, Torres VE, Ikeda Y. B-type natriuretic peptide overexpression ameliorates hepatorenal fibrocystic disease in?a?rat?model of polycystic kidney disease. Kidney Int. 2017 09; 92(3):657-668.
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Sayres LC, Magnus D. Duty-free: the non-obligatory nature of preimplantation genetic diagnosis. Am J Bioeth. 2012; 12(4):1-2.
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Vujic M, Heyer CM, Ars E, Hopp K, Markoff A, Orndal C, Rudenhed B, Nasr SH, Torres VE, Torra R, Bogdanova N, Harris PC. Incompletely penetrant PKD1 alleles mimic the renal manifestations of ARPKD. J Am Soc Nephrol. 2010 Jul; 21(7):1097-102.
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Edelstein CL. Mammalian target of rapamycin and caspase inhibitors in polycystic kidney disease. Clin J Am Soc Nephrol. 2008 Jul; 3(4):1219-26.
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Birnbaum A, Suchy FJ. The intrahepatic cholangiopathies. Semin Liver Dis. 1998; 18(3):263-9.
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