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 |
|---|
| 2005 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 1 | 2 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2021 | 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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Recent advances in understanding ion transport mechanisms in polycystic kidney disease. Clin Sci (Lond). 2021 11 12; 135(21):2521-2540.
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Salt-deficient diet exacerbates cystogenesis in ARPKD via epithelial sodium channel (ENaC). EBioMedicine. 2019 Feb; 40:663-674.
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Characterization of purinergic receptor expression in ARPKD cystic epithelia. Purinergic Signal. 2018 12; 14(4):485-497.
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Implementing Patch Clamp and Live Fluorescence Microscopy to Monitor Functional Properties of Freshly Isolated PKD Epithelium. J Vis Exp. 2015 Sep 01; (103).
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Cystic kidney disease: a primer. Adv Chronic Kidney Dis. 2015 Jul; 22(4):297-305.
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Impaired epithelial Na+ channel activity contributes to cystogenesis and development of autosomal recessive polycystic kidney disease in PCK rats. Pediatr Res. 2015 Jan; 77(1-1):64-9.
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Heightened epithelial Na+ channel-mediated Na+ absorption in a murine polycystic kidney disease model epithelium lacking apical monocilia. Am J Physiol Cell Physiol. 2006 Apr; 290(4):C952-63.