| ARPD | autosomal recessive polycystic disease |
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| ARPKD | autosomal recessive polycystic kidney disease |
| CPD | calcium pyrophosphate deposition; cephalopelvic disproportion; cerebelloparenchymal disorder; childh... |
| CPKD | childhood polycystic kidney disease |
| IPCD | infantile polycystic disease |
| polycystic kidney disease |
a genetic disorder characterized by the growth of numerous cysts filled with fluid in the kidneys.
출처: www.uchicagokidshospital.org/online-library/conten...
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| polycystic ovary syndrome |
(PCO): syndrome often characterized clinically by irregular menses, elevated circulating androgens, insulin resistance, obesity, hirsutism and in many cases anovulation and infertility. The ovaries are typically enlarged with white glossy capsules beneath which are multiple cysts in various developmental stages
출처: www.storknet.com/complications/glossary.htm
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| polycystic kidney disease |
A rare inherited condition in which the kidney are composed of multiple cysts. Kidney cysts are associated with an increased incidence of cerebral aneurysm. Symptoms usually appear later (if they do at all) and include blood in the urine, flank pain, excessive urination at night and abdominal pain. Individuals may also have elevated blood pressure. Chronic (end-stage renal disease) renal failure is the most common result in the 5th to 6th decades of life.
출처: www.talktransplant.co.uk/transcaretemplates/glossa...
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| polycystic ovary syndrome |
A condition in which cysts in the ovary interfere with normal ovulation and menstruation.
출처: boards.webmd.com/content/article/73/88004.htm
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| polycystic ovaries |
A seemingly hormonal disorder that frequently causes infertility. Small cysts formed on the ovaries is one of the most common symptoms.
출처: preconception.com/resources/glossary.htm
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