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  • ¿µ¹®
    ÇѱÛ
  • Hallervorden-Spatz syndrome
    ÇÒ·¯º¸¸£µ§-½´ÆÄÃ÷ÁõÈıº
  • hemorrhagic fever with renal syndrome
    ÃâÇ÷¿­ÄáÆÏÁõÈıº, ÃâÇ÷¿­½ÅÁõÈıº
  • hepatorenal syndrome
    °£ÄáÆÏÁõÈıº
  • hand-foot syndrome
    ¼Õ¹ßÁõÈıº
  • hantavirus pulmonary syndrome
    ÇÑŸ¹ÙÀÌ·¯½ºÆóÁõÈıº
  • Horner¡¯s syndrome
    È£³ÊÁõÈıº
  • Hunter¡¯s syndrome
    ÇåÅÍÁõÈıº
  • Hurler¡¯s syndrome
    Çæ·¯ÁõÈıº
  • iridocorneal endothelial syndrome
    ȫä°¢¸·³»ÇÇÁõÈıº
  • irritable bowel syndrome
    °ú¹Î´ëÀåÁõÈıº
  • immotile cilia syndrome
    ºÎµ¿¼¶¸ðÁõÈıº
  • impingement syndrome
    ºÎµúÈûÁõÈıº, Ãæµ¹ÁõÈıº
  • idiopathic respiratory distress syndrome
    Ư¹ßÈ£Èí°ï¶õÁõÈıº
  • intracerebral steal syndrome
    ³ú³»Ç÷·ù»©¾Ñ±èÁõÈıº
  • Jadassohn-Lewandowsky syndrome
    ¾ß´Ù½ºÁ¸-·¹¹Ýµµºê½ºÅ°ÁõÈıº
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    ÇѱÛ
  • hypoventilation syndrome
    È£ÈíÀúÇÏÁõÈıº
  • idiopathic cramp syndrome
    Ư¹ß°æ·ÃÁõÈıº
  • idiopathic respiratory distress syndrome
    Ư¹ßÈ£Èí°ï¶õÁõÈıº
  • immersion foot syndrome
    ħ¼ö¹ßÁõÈıº, ¹ß´ã±ÝÁõÈıº
  • immune amnesia syndrome
    ¸é¿ª±â¾ï»ó½ÇÁõÈıº
  • immunoproliferative syndrome
    ¸é¿ª¼¼Æ÷Áõ½ÄÁõÈıº
  • impingement syndrome
    ºÎµúÈûÁõÈıº
  • infantile stiff skin syndrome
    ¿µ¾ÆÇǺΰæÁ÷ÁõÈıº
  • interosseous nerve syndrome
    »À»çÀ̽ŰæÁõÈıº, °ñ°£½Å°æÁõÈıº
  • intersection syndrome
    ±³Â÷ÁõÈıº
  • intracerebral steal syndrome
    ³ú³»Ç÷·ùÀúÇÏÁõÈıº
  • irritable bowel syndrome
    °ú¹Î´ëÀåÁõÈıº
  • irritation syndrome
    ÀÚ±ØÁõÈıº
  • Jadassohn-Lewandowsky syndrome
    (¢¡pachyonychia congenita) ¼±Ãµ¼Õ¹ßÅéºñ´ëÁõ
  • jet lag syndrome
    ºñÇà½ÃÂ÷ÁõÈıº
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    ÇѱÛ
  • Mikulicz s syndrome
    ¹ÌÄð¸®ÁîÁõÈıº
  • Mikulicz s syndrome
    ¹ÌÄð¸®ÂêÁõÈıº.
  • Millard-Gubler syndrome
    ¹Ð¶ó-±Íºí·¯ÁõÈıº
  • Noonan s syndrome
    ´©³­ÁõÈıº.
  • OMS organic mental syndrome
    ±âÁú¼º Á¤½ÅÁõÈıº(Ðïòõàõïñãêñøý¦ÏØ)
  • OSAS=obstructive sleep apnea syndrome
    Æó¼â¼º ¼ö¸é ¹«È£Èí ÁõÈıº
  • Oasthouse syndrome
    ¿À¿ì½ºÆ®ÇϿ콺ÁõÈıº
  • Othello syndrome
    ¿À¼¿·Î ÁõÈıº
  • PANSS=Positive and Negative Syndrome Scale
    ¾ç¼º À½¼º ÁõÈıº ôµµ
  • PIE syndrome
    È£»ê±¸¼º Æóħ½À ÁõÈıº
  • PMS(postmenopausal syndrome)
    Æó°æ±â ÁõÈıº
  • PMS(premenstrual syndrome)
    ¿ù°æÀü ÁõÈıº
  • PMS.see premenstrual syndrome
    ¿ù°æÀüÁßÈıº(êÅÌèîññøý¦ÏØ)
  • Papillon-Lefervre syndrome
    ÆÄÇÇ¿ë-¸£Æäºê¸£ ÁõÈıº
  • Parinauds oculonoduler syndrome
    ÆÄ¸®³ë¾È ¸²ÇÁÀý ÁõÈıº.
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  • ¿µ¹®
    ÇѱÛ
  • adhesive syndrome
    À¯ÂøÁõÈıº
  • adrenal cortex,cushings syndrome
    Äí½ÌÁõÈıº(¡­ñøý¦ÏØ)
  • adrenal virilizing syndrome
    ºÎ½Å¼º ³²¼ºÈ­ ÁõÈıº(¡­ñøý¦ÏØ).
  • adrenogenital syndrome
    ºÎ½Å¼º±â ÁõÈıº
  • adrenogenital syndrome
    ºÎ½Å¼º±â(ÜùãìàõÐï)ÁõÈıº
  • adrenogenital syndrome
    ºÎ½Å¼º±âÁõÈıÙ(¡­àõÐïñøý¦ÏØ)
  • adrenogenital syndrome =AGS
    ºÎ½Å¼º±âÁõÈıº(¡­àõÐïñøý¦ÏØ).
  • adrenosympathetic syndrome
    ºÎ½Å±³°¨½Å°æ(¼º) ÁõÈıº(¡­ÎßÊïãêÌèàõñøý¦ÏØ).
  • adult adrenogenital syndrome
    ¼ºÀÎ ºÎ½Å ¼º±â ÁõÈıº
  • adult respiratory distress syndrome
    ¼ºÀμº È£Èí°ï¶õÁõÈıº(à÷ìÑàõû¼ýåÍÝÑññøý¦ÏØ).
  • adult respiratory distress syndrome(ards)
    ¼ºÀμºÈ£Èí°ï¶õÁõÈıº(à÷ìÑàõû¼ýåÍÝÑññøý¦ÏØ)
  • advanced sleep phase syndrome
    ÀüÁø¼º ¼ö¸éÀ§»ó ÁõÈıº
  • aeroadaptation syndrome
    Ç×°ø¼øÀÀÁõÈıº(̰˭ËàËô̷̡˴).
  • afferent loop syndrome
    ¼öÀÔ°¢ÁõÈıº.
  • aids=£¾acquired immune deficiency syndrome
    ÈÄõ¼º¸é¿ª°áÇÌÁõÈıº(ý­ô¸àõØóæ¹ÌÀù¹ñøý¦ÏØ)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 12
AIS Abbreviated Injury Scale; amniotic infection syndrome; androgen insensitivity syndrome; anterior int...
AS acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis...
BLS bare lymphocyte syndrome; basic life support; blind loop syndrome; blood and lymphatic system; blood...
BS Bachelor of Science; Bachelor of Surgery; Bacillus subtilis; Bartter syndrome; base strap; bedside; ...
CAS calcarine sulcus; calcific aortic stenosis; Cancer Attitude Survey; carbohydrate-active steroid; car...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 12
MST Multiple subpial transection
mwh Multiple wing hair
MQMAS Multiple-Quantum Magic-Angle Spinning
MFD Multiple-fraction-per-day
SMM Smoldering multiple myeloma
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • Crigler-Najjar syndrome
    Å©¸®±Û·¯-³ª¾ß ÁõÈıº
  • Crouzon syndrome
    Å©·ÎÁ¸ ÁõÈıº, Å©·çÁ¸ ÁõÈıº
    µÎ°³ ¾È¸é À̰ñÁõ, Å©·çÁ¸¾¾ Áúȯ, ¿¡ÆÛÆ® Å©·çÁ¸¾¾ ÁõÈıº µîÀÌ µ¿ÀǾî·Î ¾²À̰í ÀÖ´Ù. µÎ°³ ±âÇü, ¾È¸é Áß¾ÓºÎÀÇ Çü¼º ºÎÀü ¹× ¾èÀº ¾È¿Í·Î ÀÎÇÑ ¾È±¸ µ¹ÃâÁõÀ» Ư¡À¸·Î ÇÑ´Ù.
  • CRST syndrome
    CRST ÁõÈıº
    Calcinosis, Raynauds
  • Cushing's syndrome
    Äí½Ì ÁõÈıº
    1. ºÎ½Å ÇÇÁúÀÇ Á¾¾ç ¶Ç´Â °úÇÕ¼º¿¡ ÀÇÇØ ÄÚ¸£Æ¼Á¹ÀÌ Áö³ªÄ¡°Ô ºÐºñµÊÀ¸·Î½á »ý±ä´Ù. º¸¸§´Þ°ú °°Àº ¾ó±¼ ¸ð½À, ¾È¸é È«Á¶, ÆÄÆÈ·ÎÇü ºñ¸¸, ¼±Ãµ¼º ÇǺμ±¿°, °íÇ÷¾Ð µîÀÌ Æ¯Â¡ÀÖ´Â Áõ»óÀÌ´Ù. 2. ºÎ½Å ÇÇÁú¿¡¼­ ´çÁú ÄÚ¸£Æ¼ÄÚÀ̵尡 °ú´ÙÇÏ°Ô ºÐºñµÇ´Â º´. 1932³â ¹Ì±¹ÀÇ H. Äí½ÌÀÌ ¹ß°ßÇÏ¿´´Ù. ºÎ½Å ÇÇÁú¿¡ ¾Ç¼º ¶Ç´Â ¾ç¼ºÀÇ Á¾¾çÀÌ »ý±â°Å³ª ºÎ½Å ÇÇÁú ±× ÀÚü°¡ °ú´ÙÇÏ°Ô Áõ½ÄÇÏ´Â °æ¿ì¿¡ ³ªÅ¸³­´Ù. ºñ±³Àû µå¹® Áõ»óÀ¸·Î, 10¡­20´ë¿¡ ¸¹°í ¿©ÀÚ¿¡°Ô ¸¹´Ù. Áõ¼¼·Î´Â °íÇ÷¾Ð, ¸¸¿ù»ó ¾È¸ð
  • Cushingoid syndrome
    Äí½Ì¾ç ÁõÈıº
  • cystic duct syndrome
    ´ã³¶ °ü ÁõÈıº
  • de Clerambault syndrome
    ²ô·¹¶ûº¸¿À ÁõÈıº
  • de-toni-Debre-Fanconi syndrome
    µð-Åä´Ï-µðºê¸®-ÆÇÄÚ´Ï ÁõÈıº
  • Defibrillation syndrome
    Å»¼¶À¯¼Ò ÁõÈıº
  • deficient antibody syndrome
    Ç×ü °áÇÌ ÁõÈıº
  • deficit syndrome
    °áÇÌ ÁõÈıº
  • Demons-Meigs' syndrome
    µ¥¸ó½º-¸Þ±×½º ÁõÈıº
    ³­¼Ò ¼¶À¯Á¾À¸·Î È÷½ºÅ¸¹Î¿¡ ÀÇÇÑ ¾Æ³ªÇʶô½Ã Áõ»ó. ¼ö´ë»ç¿Í ±³Áú°èÀÇ º´º¯ ¹× Á¾¾çÀÇ È£¸£¸ó ÀÛ¿ë¿¡ ÀÇÇØ º¹¼ö¿Í Èä¼ö°¡ º´¹ßÇÑ´Ù.
  • denial-of-deficit syndrome
    °áÇÌ ºÎÁ¤ ÁõÈıº
  • Denny-Brown's syndrome
    µ¥´Ï-ºê¶ó¿î ÁõÈıº
    ³»°æµ¿¸Æ Æó»öÁõÀ̶ó°íµµ Çϸç, ºñ±³Àû ÀþÀº Ãþ¿¡ ¸¹Àº º´À¸·Î, °£Áú ºñ½ÁÇÑ ¹ßÀÛ, °¡º­¿î ¾ð¾î ÀåÇØ, ¹Ý½Å ºÒ¼ö µîÀÇ Áõ»óÀÌ Æ¯Â¡Àε¥, ³úµ¿¸Æ ÃÔ¿µÀ¸·Î °æµ¿¸ÆÀÇ Æó»öÀ» Áõ¸íÇÒ ¼ö ÀÖ´Ù.
  • dermatorheumatismal syndrome
    ÇǺΠ·ù¸¶Æ¼½º ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 12
bare lymphocyte syndrome <syndrome> Absence of HLA antigens on peripheral mononuclear cells, which may result in immunodeficiency.
(05 Mar 2000)
Barlow's syndrome <syndrome> Also referred to as mitral valve prolapse, systolic click-murmur syndrome, floppy-valve syndrome and billowing mitral leaflet syndrome. A common, but highly variable (most individuals are asymptomatic), clinical syndrome that has been described in up to 7% of all females in the 14 to 30 age group. There is also an increased familial incidence suggesting an autosomal dominant form of inheritance.
(27 Sep 1997)
Barlow syndrome <syndrome> Late apical systolic murmur or (so-called "mid-late") systolic click, or both, due to massive billowing of the anterior and/or posterior (mural) mitral valvular leaflet into the left atrial cavity (also, floppy valve syndrome); electrocardiographically, ST-T changes in a posteroinferior distribution resembling those of myocardial ischemia often coexist for unknown reasons; rhythm disturbances may coexist with this syndrome without demonstrable pathogenetic relationship.
(05 Mar 2000)
Barrett's syndrome <syndrome> Chronic peptic ulceration of the lower oesophagus, which is lined by columnar epithelium, resembling the mucosa of the gastric cardia, acquired as a result of long-standing chronic oesophagitis; oesophageal stricture with reflux, and adenocarcinoma, also have been reported.
Synonym: Barrett's oesophagus.
(05 Mar 2000)
Bart's syndrome <syndrome> A form of epidermolysis bullosa with blistering of the extremities and intertriginous areas, erosions of the mouth, and deformed nails; probably autosomal dominant; there is often spontaneous improvement with no residual scarring.
(05 Mar 2000)
Bartter's syndrome <syndrome> A clinical syndrome characterised by enlargement of certain kidney cells, alkalosis, hypokalaemia and increased production of the hormone aldosterone. Common in children and may be seen in dwarfism.
(27 Sep 1997)
basal cell nevus syndrome <syndrome> An inherited group of defects which involve abnormalities of the skin, eyes, nervous system, endocrine, glands and bones.
The condition is characterised by an unusual facial appearance and a predisposition for skin cancer.
(27 Sep 1997)
Basan's syndrome <syndrome> Ectodermal dysplasia with hypotrichosis, hypohidrosis, defective teeth, and unusual dermatoglyphics.
(05 Mar 2000)
Bassen-Kornzweig syndrome <syndrome> A rare congenital disorder that causes the body to not produce chylomicrons, low density lipoprotein (LDL) and very low density lipoprotein (VLDL). Individuals with this condition are unable to properly digest fats. Other findings include ataxia, peripheral neuropathy and other forms of nerve dysfunction.
Treatment includes vitamin E.
(27 Sep 1997)
battered child syndrome <radiology> Multiple assymetrical fractures, separation of distal epiphyses, irregularity and fragmentation of metaphyses, bucket-handle fracture, corner fracture of elbow, knee, ankle (sudden twisting motion), isolated spiral fracture, extensive periosteal reaction (subperiosteal haemorrhage), exuberant callus formation, cortical hyperostosis extending to epiphyseal plate, avulsion fracture at ligamentous insertion, subdural haematoma (most common), brain atrophy (up to 100%), infarction (50%), subdural hygroma, encephalomalacia, porencephaly
(12 Dec 1998)
battered spouse syndrome <syndrome> Physical, psychological, and emotional injuries in a person subjected to abuse by a spouse or domestic partner; usually associated with alcoholism in the abusing spouse.
(05 Mar 2000)
Bauer's syndrome <syndrome> Aortitis and aortic endocarditis as a little recognised manifestation of rheumatoid arthritis.
(05 Mar 2000)
Bazex's syndrome <syndrome> Erythematous to plum-coloured scaly acral skin lesions, paronychia, and nail dysplasia; associated with cancer of the upper respiratory or upper alimentary tract.
Synonym: paraneoplastic acrokeratosis.
(05 Mar 2000)
Beckwith syndrome <syndrome> This syndrome, of unknown cause, is characterised by a group of the following findings: large tongue, organ enlargement (visceromegaly), large body size, umbilical hernia and neonatal hypoglycaemia. Evidence suggests a genetic lesion. Birth weight is often more than 8 pounds. Complications include Wilm's tumour, seizures, aspiration and hypoglycaemia.
(27 Sep 1997)
Beckwith-Wiedemann syndrome <syndrome> This syndrome, of unknown cause, is characterised by a group of the following findings: large tongue, organ enlargement (visceromegaly), large body size, umbilical hernia and neonatal hypoglycaemia. Evidence suggests a genetic lesion. Birth weight is often more than 8 pounds. Complications include Wilm's tumour, seizures, aspiration and hypoglycaemia.
(27 Sep 1997)
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