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  • ¿µ¹®
    ÇѱÛ
  • progressive lingual hemiatrophy
    ÁøÇàÇô¹ÝÀ§ÃàÁõ
  • progressive mean
    ´©°¡Æò±Õ
  • progressive multifocal leukoencephalopathy
    ÁøÇà´ÙÃÊÁ¡¹é(»ö)Áú³úº´(Áõ)
  • progressive muscular dystrophy
    ÁøÇà±Ù(À°)µð½ºÆ®·ÎÇÇ
  • progressive myopia
    ÁøÇà±Ù½Ã
  • progressive nuclear ophthalmoplegia
    ÁøÇà½Å°æÇÙ´«±ÙÀ°¸¶ºñ
  • progressive outer retinal necrosis
    ÁøÇ༺¿Ü¸Á¸·±«»ç
  • progressive pigmentary dermatosis
    ÁøÇà»ö¼ÒÇǺκ´
  • progressive resistance
    Á¡ÁõÀúÇ×
  • progressive resistance exercise
    Á¡ÁõÀúÇ׿
  • progressive spastic spinal paralysis
    ÁøÇà°­Á÷ô¼ö¸¶ºñ
  • progressive spinal amyotrophy
    ÁøÇàô¼ö±Ù(À°)À§Ãà(Áõ)
  • progressive spinal muscular atrophy
    ÁøÇàô¼ö¼º±Ù(À°)À§ÃàÁõ
  • progressive subcortical encephalopathy
    ÁøÇà°ÑÁú¹Ø³úº´(Áõ), ÁøÇàÇÇÁúÇϳúº´(Áõ)
  • progressive supranuclear palsy
    ÁøÇàÇٻ󸶺ñ
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  • idiopathic muscular spasm
    Ư¹ß±ÙÀ°¿¬Ãà
  • idiopathic respiratory distress syndrome
    Ư¹ßÈ£Èí°ï¶õÁõÈıº
  • idiopathic thrombocytopenic purpura
    Ư¹ßÇ÷¼ÒÆÇ°¨¼ÒÀÚ»ö¹Ýº´
  • progressive diffuse keratoderma
    ±¤¹üÀ§ÁøÇà°¢ÁúÇǺÎÁõ
  • progressive cardiomyopathic lentiginosis
    ÁøÇà½ÉÀå±ÙÀ°º´Èæ»öÁ¡Áõ
  • progressive multifocal leukoencephalopathy
    ÁøÇà´ÙÃÊÁ¡¹é»öÁú³úÁõ
  • progressive mean
    ´©°¡Æò±Õ
  • progressive myopia
    ÁøÇà±Ù½Ã
  • progressive hypertrophic interstitial neuritis
    ÁøÇàºñ´ë»çÀÌÁú½Å°æ¿°
  • progressive nuclear ophthalmoplegia
    ÁøÇà½Å°æÇÙ´«±ÙÀ°¸¶ºñ
  • progressive
    ÁøÇà-
  • progressive bulbar palsy
    ÁøÇà¼û³ú¸¶ºñ, ÁøÇ౸¸¶ºñ
  • progressive resistance
    Á¡ÁõÀúÇ×
  • progressive thrombus
    ÁøÇàÇ÷Àü
  • progressive spastic spinal paralysis
    ÁøÇà°æÁ÷ô¼ö¸¶ºñ
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  • idiopathic thrombocytopenic purpura
    Ư¹ß¼ºÇ÷¼ÒÆÇ°¨¼Ò¼ºÀڹݺ´(¡­úìá³÷ùÊõá´àõí¹ÚèÜ»)
  • idiopathic thrombocytopenic purpura =ITP
    Ư¹ß¼º Ç÷¼ÒÆÇ °¨¼Ò¼º Àڹݺ´.
  • idiopathic unilateral hyperlucent lung
    Ư¹ß¼º ÀÏÃø¼º °úÅõ°ú¼ºÆó
  • idiopathic uveitis
    Ư¹ß¼ºÆ÷µµ¸·¿°.
  • acquired progressive lymphangioma
    ÈÄõ¼º ÁøÇ༺ ¸²ÇÁ°üÁ¾
  • hereditary progressive mucinous histiocytosis X
    À¯Àü¼º ÁøÇ༺ Á¡¾×¼ºÁ¶Á÷±¸Áõ
  • infantile progressive spinal muscular atrophy
    ¿µ¾ÆÁøÇ༺ ô¼ö¼º ±ÙÀ§Ãà(Áõ).
  • progressive
    ÁøÇ༺
  • progressive
    ÁøÇ༺ÀÇ(òäú¼àõ¡­), Á÷Áø(¼º)ÀÇ(òÁòä(àõ)¡­)
  • progressive bulbar palsy
    ÁøÇ༺ ±¸<¿¬¼ö>¸¶ºñ(òäú¼àõϹ<æÅâÐ> Ýö).
  • progressive cardiomyopathic lentiginosis
    ÁøÇ༺ ½É±Ùº´¼º ÈæÀÚÁõ
  • progressive case
    ÁøÇ༺ ¿¹.
  • progressive deafness
    ÁøÇà(¼º) ³­Ã»
  • progressive deafness
    ÁøÇ༺ ³­Ã»(òäú¼àõ Ññôé)
  • progressive diaphyseal dysplasia
    ÁøÇ༺ °ñ°£¼º ÀÌÇü¼º(Áõ)(òäú¼àõÍéÊÏàõì¶ û¡à÷ñø).
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  • idiopathic esophaegal dilatation
    Ư¹ß¼º ½ÄµµÈ®Àå(Áõ).
  • idiopathic esophageal achalasia
    Ư¹ß¼º ½Äµµ°æ·ÃÁõ.
  • idiopathic esophageal achalasia
    Ư¹ß¼º ½Äµµ°æ·ÃÁõ
  • idiopathic esophageal dilatation
    Ư¹ß¼º ½ÄµµÈ®Àå(Áõ).
  • idiopathic facial paralysis
    Ư¹ß¼º ¾È¸é½Å°æ¸¶ºñ.
  • idiopathic facial paralysis
    Ư¹ß¼º ¾È¸é½Å°æ¸¶ºñ
  • idiopathic familial fibromatosis
    Ư¹ß¼º °¡Á·¼º ¼¶À¯Á¾Áõ.
  • idiopathic familial fibromatosis
    Ư¹ß¼º °¡Á·¼º ¼¶À¯Á¾Áõ
  • idiopathic hemochromatosis
    Ư¹ß¼º Ç÷ö ¼ÒÁõ.
  • idiopathic hemorrhagic sarcoma
    Ư¹ß¼º ÃâÇ÷¼º À°Á¾
  • idiopathic hypercalciuria
    Ư¹ß¼º °íÄ®½· ´¢(Áõ).
  • idiopathic hyperkinetic heart syndrome
    Ư¹ß¼º °ú¿îµ¿¼º ½ÉÁõÈıº.
  • idiopathic hypertrophic osteoarthropathy
    Ư¹ß¼º °úÇü¼º °ñ°üÀýº´Áõ.
  • idiopathic hypertrophic osteoarthropathy
    Ư¹ß¼º °ñ ´Ù°øÁõ(÷åÛ¡àõÍéÒýÍîñø), Ư¹ß¼º °ñ Á¶¼ÛÁõ(÷åÛ¡àõÍéðØáçñø), Ư¹ß¼º °úÇü¼º °ñ°üÀýº´Áõ.
  • idiopathic hypertrophic subaortic stenosis
    Ư¹ß¼º ºñÈļº ´ëµ¿¸ÆÆÇ ÇϺÎÇùÂø(Áõ).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 5
AION anterior ischemic optic neuropathy
AN acanthosis nigricans; acne neonatorum; acoustic neuroma; adult, normal; ala nasi; amyl nitrate; aneu...
BPN bacitracin, polymyxin B, neomycin sulfate; brachial plexus neuropathy
CSNA congenital sensory neuropathy with anhidrosis [syndrome]
DN Deiter's nucleus; dextrose-nitrogen; diabetic neuropathy; dibucaine number; dicrotic notch; dinitroc...
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PN Peripheral neuropathy
SMON Subacute Myelo-Optico-Neuropathy
HMSN hereditary motor sensory neuropathy
NAION non-arteritic ischaemic optic neuropathy
CPEO Chronic Progressive External Ophthalmoplegia
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idiopathic neuralgia <symptom> Nerve pain not due to any apparent cause.
(05 Mar 2000)
idiopathic orthostatic hypotension <clinical sign> The tendency for blood pressure to drop for unknown reasons on assuming upright posture.
(05 Mar 2000)
idiopathic paroxysmal rhabdomyolysis Excretion of myoglobin in the urine; results from muscle degeneration, which releases myoglobin into the blood; occurs in certain types of trauma (crush syndrome), advanced or protracted ischemia of muscle, or as a paroxysmal process of unknown aetiology.
Synonym: idiopathic paroxysmal rhabdomyolysis, Meyer-Betz disease, Meyer-Betz syndrome.
(05 Mar 2000)
idiopathic proctitis Probably a variant of ulcerative colitis involving the rectum; some cases progress to involve the remainder of the colon as well.
Synonym: chronic ulcerative proctitis.
(05 Mar 2000)
idiopathic pulmonary fibrosis <radiology> Aka: usual interstitial pneumonia (UIP), 5-6th decade; M:F = 1:1, clubbing of fingers (83%), lymphocytosis on lavage, increased occurence of bronchogenic CA, average survival of 4-6 years; 87% mortality CXR findings: occasional ground glass pattern in early stage of alveolitis, diffuse reticulations (60%) predominantly at bases, honeycombing, pleural effusion (4%); pleural thickening (6%), pneumothorax in 7% (late stage), progressive volume loss see: interstitial pulmonary fibrosis
(12 Dec 1998)
idiopathic pulmonary haemosiderosis <chest medicine> A rare, sporadic, fatal, mostly in children with an equal sex distribution.
The condition also occurs in adults where there is a sex difference (M:F = 2:1). The patients present with recurrent attacks of pulmonary haemorrhage, acute phase: bat-wing alveolar infiltrates, clears rapidly, chronic findings: haemosiderosis, pulmonary fibrosis, cor pulmonale.
(12 Dec 1998)
idiopathic pulmonary hypertension <chest medicine> A condition where there is increased blood pressure in the pulmonary arteries with otherwise normal heart and lungs.
The cause is unknown, but there is diffuse narrowing of the pulmonary arteries resulting in increased arteriolar pressures. Secondary heart failure ensues without correction of this problem. There is an increased incidence of this disease in females between the ages of 20 and 40 years. Treatment may include a heart and lung transplant in select cases.
(27 Sep 1997)
idiopathic roseola Roseola not occurring as a symptom of a recognised general disease.
(05 Mar 2000)
idiopathic thrombocytopenia purpura <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding.
The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin.
Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients.
Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form.
Acronym: ITP
(20 Sep 2002)
idiopathic thrombocytopenic purpura <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding.
The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin.
Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients.
Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form.
Acronym: ITP
(20 Sep 2002)
dystonia, idiopathic torsion A form of dystonia known as early-onset torsion dystonia (also called generalised torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating.
(12 Dec 1998)
t-lymphocytopenia, idiopathic CD4-positive Reproducible depletion of CD4+ lymphocytes below 300 per cubic millimeter in the absence of HIV infection or other known causes of immunodeficiency. This is a rare, heterogeneous syndrome and does not appear to be caused by a transmissible agent.
(12 Dec 1998)
jaundice, chronic idiopathic A familial chronic form of nonhemolytic jaundice thought to be due to a defect in the excretion of conjugated bilirubin and certain other organic anions (e.g., sulfobromophthalein) by the liver. It is characterised by the presence of a brown, coarsely granular pigment in the hepatic cells, which is pathognomonic of the condition.
(12 Dec 1998)
Leber's idiopathic stellate neuroretinitis A unilateral neuroretinitis with perifoveal exudates in Henle's nerve fibre layer producing a macular star and spontaneous regression in a few months.
Synonym: Leber's idiopathic stellate neuroretinitis.
(05 Mar 2000)
Leber's idiopathic stellate retinopathy An inflammation affecting the optic nerve head and the posterior pole of the retina, with cells in the nearby vitreous, usually producing a macular star.
Synonym: papilloretinitis.
(05 Mar 2000)
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