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First, prefixes and suffixes, most of which are derived from ancient Greek or classical Latin, have a droppable vowel, usually -o-. As a general rule, this vowel almost always acts as a joint-stem to connect two consonantal roots (e.g. arthr- + -o- + -logy = arthrology ), but generally, the -o- is dropped when connecting to a vowel-stem (e.g ...
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 childhood, or in adulthood. [8]
The term is from Greek πύελο|ς pýelo|s, "basin" + νεφρ|ός nepʰrós, "kidney" + suffix -itis suggesting "inflammation". [citation needed] A similar term is "pyelitis", which means inflammation of the renal pelvis and calyces. [39] [40] In other words, pyelitis together with nephritis is collectively known as pyelonephritis ...
Creutzfeldt–Jakob disease: CKD Chronic kidney disease: CLOVES syndrome Congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and skeletal/spinal abnormalities syndrome CML Chronic myelogenous leukemia: CMs Chiari malformations: CMT disease Charcot–Marie–Tooth disease: CMT1A Charcot–Marie–Tooth disease type 1A CMT1B
Among American patients on the kidney-transplant waiting list (as of December 2011), 7256 (8.4%) were listed due to cystic kidney disease and of the 16,055 renal transplants performed in 2011, 2057 (12.8%) were done for patients with cystic kidney disease, with 1,189 from deceased donors and 868 from living donors. [80]
polycystic kidney disease: PKP: penetrating keratoplasty: PKU: phenylketonuria (PKU card—see Guthrie test) PLAT: tissue plasminogen activator: PLIF: posterior lumbar interbody fusion (a type of spinal fusion) PLT: platelets: PM: post meridiem (in the afternoon) PMB: post-menopausal bleeding (bleeding after menopause) PMD: primary medical ...
Cystic kidney disease includes various conditions related to the formation of cysts in one or both kidneys. The most common subset is polycystic kidney disease (PKD), which is a genetic anomaly with two subsets, autosomal recessive polycystic kidney disease (ARPKD) and autosomal dominant polycystic kidney disease (ADPKD).
Polycystic kidney disease, adult type; Polycystic kidney disease, infantile type; Polycystic kidney disease, infantile, type I; Polycystic kidney disease, recessive type; Polycystic kidney disease, type 1; Polycystic kidney disease, type 2; Polycystic kidney disease, type 3; Polycystic kidney disease; Polycystic ovarian disease, familial ...