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| ¿µ¹® | renal transplantation | ÇÑ±Û | ÄáÆÏÀÌ½Ä |
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| ¿µ¹® | testicular feminization syndrome | ÇÑ±Û | °íȯ¿©¼ºÈÁõÈıº |
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| FS | factor of safety; Fanconi syndrome; Felty syndrome; fibromyalgia syndrome; field stimulation; Fisher... |
|---|---|
| MS | Maffuci syndrome; maladjustment score; mandibular series; Marfan syndrome; Marie-Strumpell [syndrome... |
| RS | radioscaphoid; random sample; rating schedule; Raynaud syndrome; recipient's serum; rectal sinus; re... |
| AFS | acquired or adult Fanconi syndrome; alternative financing system; American Fertility Society; antifi... |
| FAZ | Fanconi-Albertini-Zellweger [syndrome]; foveal avascular zone; fragmented atrial activity zone |
| FS | Fanconi syndrome |
|---|---|
| FA | Fanconi Anemia |
| HFRS | Haemorrhagic Fever with Renal Syndrome |
| HFRS | Hemorrhagic fever with the renal syndrome |
| CHRS | cerebro-hepato-renal syndrome |
| De Toni-Fanconi syndrome | Lysosomal storage disorders of unknown molecular defect, characterised by widespread deposition of cystine crystals in reticuloendothelial cells. (12 Dec 1998) |
|---|---|
| Fanconi's syndrome | <syndrome> A group of conditions with characteristic disorders of renal tubular function, which may be classified as: 1. Cystinosis, an autosomal recessive disease of early childhood. 2. Adult Fanconi syndrome, a rare hereditary form, probably due to a recessive gene different from that found in cystinosis, characterised by the tubular malfunction seen in cystinosis and by osteomalacia, but without cystine deposit in tissues. 3. Acquired Fanconi syndrome, which may be associated with multiple myeloma or may result from chemical poisoning, injury, or persisting damage of proximal tubular epithelium due to various causes, leading to multiple defects of tubular function. (05 Mar 2000) |
| Fanconi syndrome | <syndrome> Transport disease (recessive defect) in which the renal reabsorption of several substances (phosphate, glucose, amino acids) is impaired. (18 Nov 1997) |
| Lignac-Fanconi syndrome | Lysosomal storage disorders of unknown molecular defect, characterised by widespread deposition of cystine crystals in reticuloendothelial cells. (12 Dec 1998) |
| pancytopenia, fanconi | A genetic (inherited) disease with progressive decline in blood cells and a tendency to leukaemia. Also known as fanconi anaemia. (12 Dec 1998) |
| Fanconi, Guido | <person> Swiss paediatrician, 1892-1979. See: Fanconi's anaemia, Fanconi's pancytopenia, Fanconi's syndrome, De Toni-Fanconi syndrome, Lignac-Fanconi syndrome. (05 Mar 2000) |
| Fanconi's anaemia | <haematology> A rare inherited type of aplastic anaemia which carries an increased risk to the patient of developing leukaemia. May be treated by bone marrow transplant. Origin: Gr. Haima = blood (13 Nov 1997) |
| Fanconi's pancytopenia | fanconi's anaemia |
| branchio-oto-renal syndrome | <syndrome> An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to mondini type cochlear defect and stapes fixation. (12 Dec 1998) |
| haemorrhagic fever with renal syndrome | <syndrome> An acute febrile disease occurring predominately in asia. It is characterised by fever, prostration, vomiting, haemorrhagic phenonema, shock, and renal failure. It is caused by any one of several closely related species of the genus hantavirus. The most severe form is caused by hantaan virus whose natural host is the rodent apodemus agrarius. A milder form is caused by seoul virus and related species and transmitted by the rodents rattus rattus and r. Norvegicus. (12 Dec 1998) |
| acute renal failure | <nephrology> A sudden decline in renal function may be triggered by a number of acute disease processes. Examples include sepsis (infection), shock, trauma, kidney stones, kidney infection, drug toxicity (aspirin or lithium), poisons or toxins (drug abuse) or after injection with an iodinated contrast dye (adverse effect). Chronic renal failure represents a slow decline in kidney function over time. Chronic renal failure may be caused by a number of disorders which include long-standing hypertension, diabetes, congestive heart failure, lupus or sickle cell anaemia. Both forms of renal failure result in a life-threatening metabolic derangement. (27 Sep 1997) |
| aminoaciduria, renal | Impairment of renal tubular transport of amino acids. (12 Dec 1998) |
| back-pressure renal atrophy | <radiology> Caliectasis without obstruction, due to repeated episodes of obstruction, gradual loss of renal pyramids (12 Dec 1998) |
| base of renal pyramid | The outer broad part of a renal pyramid that lies next to the cortex. Synonym: basis pyramidis renis. (05 Mar 2000) |
| capsular branches of renal artery | <anatomy, artery> Branches arising from the renal artery outside of the kidney that are distributed to the renal capsule. Synonym: rami capsulares arteriae renalis. (05 Mar 2000) |
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