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  • ¿µ¹®
    ÇѱÛ
  • 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
  • jet lag syndrome
    ½ÃÂ÷ÁõÈıº
  • Kallmann syndrome
    Ä®¸¸ÁõÈıº
  • Kartagener¡¯s syndrome
    Ä«¸£Å¸°Ô³ÊÁõÈıº
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    ÇѱÛ
  • 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
  • lazy bladder syndrome
    °ÔÀ¸¸§¹æ±¤ÁõÈıº
  • locked-in syndrome
    °¨±ÝÁõÈıº
  • lymphadenopathy syndrome
    ¸²ÇÁÀýº´ÁõÁõÈıº
  • lymphoproliferative syndrome
    ¸²ÇÁÁõ½ÄÁõÈıº
  • malabsoption syndrome
    Èí¼öÀå¾ÖÁõÈıº
  • maladaptation syndrome
    ÀûÀÀÀå¾ÖÁõÈıº
  • maltreatment syndrome
    ÇдëÁõÈıº
  • maternal deprivation syndrome
    ¸ð¼º¹ÚÅ»ÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • Klinefelters syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº
  • Klinefelters syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº(¡­ñøý¦ÏØ)
  • Klippel Feli syndrome
    Ŭ¸®Æç-ÆäÀÏÁõÈıº.
  • Lambert-Eaton myasthenic syndrome
    ¶÷¹öÆ®-ÀÌÆ° ±Ù¹«·ÂÁõÁõÈıº
  • Landry Guillain Barre syndrome
    ¶õµå¸®-±æ·©-¹Ù·¹ÁõÈıº.
  • Laurence Moon Biedl syndrome
    ·Î·»½º-¹®-ºñµéÁõÈıº.
  • Lesch-Nyhan syndrome
    ·¹½¬ ´ÏÇÑ ÁõÈıº
  • Leser-Trelat syndrome
    ·¹Á¦¸£ Æ®·¼¶ó ÁõÈıº
  • Lhermittes syndrome, radiation-induced
    ¹æ»ç¼±À¸·Î À¯¹ßµÈ ·¹¹ÌÅ× ÁõÈıº
  • Libman Sachs syndrome
    ¸®ºê¸¸-ÀÛ½º ÁõÈıº.
  • Loeffler s eosinophilic syndrome
    ·ÚÇ÷¯È£»ê±¸ÁõÈıº
  • Loeffler s eosinophilic syndrome
    ·ÚÇ÷¯È£»ê±¸ÁõÈıº.
  • Loefflers syndrome
    ·ÚÇ÷¯ÁõÈıº
  • Lofgrens syndrome
    ·ÚÇÁ ±×¸° ÁõÈıº
  • Marchesanis syndrome
    ¸¶¸£ÄÉ»ç´ÏÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • 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)
  • albrights syndrome
    ¾ËºÎ¶óÀÌÆ® ÁõÈıº(¡­ñøý¦ÏØ)
  • alports syndrome
    ¾ËÆ÷¿ÀÆ®ÁõÈıº
  • alports syndrome(disease)
    ¾ËÆ÷Æ® ÁõÈıº(º´)(¡­ñøý¦ÏØ)
  • alveolar hypoventilation syndrome
    ÆóÆ÷Àúȯ±âÁõÈıº.
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TS Takayasu syndrome; Tay-Sachs; temperature sensitivity; temperature, skin; temporal stem; tensile str...
L/E Lower Extremity
LES Lower Esophageal Sphincter; ÇϺΠ½Äµµ °ý¾à±Ù
LESP Lower Esophageal Sphincter Prssure
LLL Left Lower Lobe(of Lung)
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AIDS Acquired Immune Deficiency Disease Syndrome
AVWS Acquired von Willebrand syndrome
ARDS Acute respiratory distress syndrome
ACS Acute Chest Syndrome
ARN Acute retinal necrosis syndrome
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    ¼³¸í
  • congenital rubella syndrome
    ¼±Ãµ¼º dzÁø ÁõÈıº
    žư¡ ¸ðü ³»¿¡¼­ dzÁø ¹ÙÀÌ·¯½º¿¡ Ä§ÇØµÇ¾î »ý±â´Â ÀÌ»ó Áõ¼¼. ÀӽŠÃʱâÀÇ ÀÓ»êºÎ°¡ dzÁø¿¡ °É¸®¸é žư¡ ¹ßÀ° Ãʱ⿡ dzÁø ¹ÙÀÌ·¯½º¿¡ Ä§ÇØµÇ¾î Ãâ»ý ÈÄ¿¡ ´«ÀÇ ÀÌ»ó
  • conjunctivo-urethro-synovial syndrome
    °á¸· ´¢µµ Ȱ¸· ÁõÈıº
  • Conn syndrome
    ÄÜ ÁõÈıº
  • contiguous gene syndrome
    Á¢Ã˼º À¯ÀüÀÚ ÁõÈıº
  • cord compression syndrome
    ô¼ö ¾Ð¹Ú ÁõÈıº
  • corpus callosum syndrome
    ³ú·® ÁõÈıº
  • Cowden syndrome
    ÄÚ¿ìÅÙ ÁõÈıº
    ½Å»ý¹° ÁõÈıº. À¯µÎÁ¾°ú ºñ½ÁÇÑ º´¼Ò·Î ÀÚ°¥°°Àº ÇüÅÂÀÎ ¼¶µàÁ¾ÀÌ´Ù.
  • cracked tooth syndrome
    ±Õ¿­Ä¡ Áõ»ó, ±Õ¿­Ä¡ ÁõÈıº, ÆÄÀýÄ¡ ÁõÈıº
  • cranial nerve syndrome
    ³ú½Å°æ ÁõÈıº
  • cri du chat syndrome
    ¹¦¼º ÁõÈıº
    Á¦ 5¹ø ¿°»öüÀÇ ´Ü¿ÏÀÇ ÀϺΰ¡ °á¼ÕµÇ¾î ³ªÅ¸³ª´Â À¯Àü¼º ¼±Ãµ¼º ÁõÈıºÀ¸·Î, ¾ç¾È °Ý¸®Áõ, ¼ÒµÎÁõ, ½ÉÇÑ Á¤½Å¹Ú¾àÁõ, °í¾çÀÌ °°Àº ¿ïÀ½¼Ò¸®¸¦ Ư¡À¸·Î ÇÑ´Ù.
  • 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
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 10
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)
Behcet's syndrome <syndrome> A multisystem, chronic recurrent disease characterised by ulceration in the mouth and genitalia, iritis, uveitis, arthritis and thrombophlebitis. Often treated with immunosuppressive therapy (corticosteroids, chlorambucil).
(27 Sep 1997)
Behr's syndrome <syndrome> Adult or presenile form of heredomacular degeneration.
Synonym: Behr's disease.
(05 Mar 2000)
Benedikt's syndrome <syndrome> Hemiplegia with clonic spasm or tremor and oculomotor paralysis on the opposite side.
(05 Mar 2000)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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