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  • ¿µ¹®
    ÇѱÛ
  • 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
  • Klinefelter¡¯s syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº
  • Klippel-Feil syndrome
    Ŭ¸®Æç-ÆÄÀÏÁõÈıº
  • Korsakoff¡¯s syndrome
    ÄÚ¸£»çÄÚÇÁÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • hyperviscosity syndrome
    °ú´ÙÁ¡¼ºÁõÈıº
  • 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
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  • ¿µ¹®
    ÇѱÛ
  • 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
  • Marcus-Gunn syndrome
    ¸¶¸£Äí½º-°ÇÁõÈıº
  • Marfan s syndrome
    ¸¶¸£ÆÎÁõÈıº
  • Marfan s syndrome
    ¸¶¸£ÆÎÁõÈıº.
  • Marfans syndrome
    ¸¶¸£ÆÎÁõÈıº.
  • Marfans syndrome
    ¸¶¸£ÆÎ ÁõÈıº.
  • McLeod syndrome
    ¸Æ·¹¿ÀÁõÈıº
  • Melkersson-Rosenthal syndrome
    ¸áÄ¿½¼ ·ÎÁ¨Å» ÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • anterolateral syndrome
    ô¼öÀüÃø°¢ÁõÈıº(ô±âÐîñö°ÊÇñøý¦ÏØ).
  • antibody deficiency syndrome
    Ç×ü°áÇÌÁõÈıº(ù÷ô÷ÌÀù¹ñøý¦ÏØ).
  • anticardiolipin syndrome
    Ç×Ä«¸£µð¿Ã¸®ÇÉÁõÈıº
  • anticardiolipin syndrome
    Ç×Ä«µð¿À¸®ÇÉÁõÈıº
  • antiphospholipid syndrome
    Ç×ÀÎÁöÁúÁõÈıº
  • anxiety syndrome
    ºÒ¾ÈÁõÈıº(¡­ñøý¦ÏØ).
  • aortic arch syndrome
    ´ëµ¿¸Æ±ÃÁõÈıº(¡­ñøý¦ÏØ).
  • aortic arch syndrome
    ´ëµ¿¸Æ±Ã ÁõÈıº(¡­Ïáñøý¦ÏØ)
  • aortitis syndrome
    ´ëµ¿¸Æ¿°ÁõÈıº(¡­æúñøý¦ÏØ).
  • aortitis syndrome
    ´ëµ¿¸Æ¿° ÁõÈıº(¡­ñøý¦ÏØ)
  • apallic syndrome
    ¹«½ÉÁõÈıº(Ùíãýñøý¦ÏØ)
  • apathetic-akinetic syndrome
    ¹«°¨µ¿-¹«µ¿ÀÛ ÁõÈıº
  • aphasic and apraxic syndrome
    ½Ç¾î½ÇÇàÁõÈıº(ã÷åÞãùú¼ñøý¦ÏØ).
  • aqueous mis-direction syndrome
    ¹æ¼öÈ帧ÀÌ»óÁõÈıº
  • ards(adult respiratory disress syndrome)
    ARDS(¼ºÀÎÈ£Èí°ï¶õÁõÈıº)(à÷ìÑû¼ýåÍÝÑññøý¦ÏØ)
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GS gallstone; Gardner syndrome; gastric shield; general surgery; gestational score; Gilbert syndrome; g...
HSS Hallermann-Streiff syndrome; Hallervorden-Spatz syndrome; Henoch-Schonlein syndrome; high-speed supe...
MAS magic angle spinning; Manifest Anxiety Scale; maximum average score; McCune-Albright syndrome; mecon...
MDS Master of Dental Surgery; maternal deprivation syndrome; medical data screening; medical data system...
OHS obesity hypoventilation syndrome; occipital Horn syndrome; occupational health service; ocular histo...
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HSR heat shock response
HSTF heat shock transcription factor
MDS 7--myelodysplastic syndrome
ACS Abdominal compartment syndrome
AIDS Acquire Immune Deficiency Syndrome
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • double crush syndrome
    ÀÌÁß ºÐ¼â ÁõÈıº
  • Dresslers syndrome
    µå·¹½½·¯ ÁõÈıº
  • Duanes retraction syndrome
    µà¾È ¾È±¸ ÈÄÅð ÁõÈıº
  • dysconnection syndrome
    ºÐ¸® ÁõÈıº
  • dyskinetic syndrome
    ¿îµ¿ Àå¾Ö ÁõÈıº
  • dysplastic nevus syndrome
    ÀÌÇü¼º ¸ð¹Ý ÁõÈıº
  • dysuria-pyuria syndrome
    ¹è´¢ Àå¾Ö-³ó´¢ ÁõÈıº
  • early postprandial postgastrectomy syndrome
    Á¶±â ½ÄÈļº À§ ÀýÁ¦ ÈÄ ÁõÈıº
  • eaton-lambert syndrome
    ÀÌÆ°-¶÷¹öÆ® ÁõÈıº
  • ectopic ACTH syndrome
    À̼Ҽº ºÎ½Å ÇÇÁú ÀÚ±Ø È£¸£¸ó ÁõÈıº, À̼Ҽº ACTH ÁõÈıº
    ACTHÀÇ °úÀ× »ý»ê, Á߽ɼº ºñ¸¸, ¸¸¿ùÇü ¾ó±¼, °íÇ÷¾Ð µîÀÇ Áõ»óÀÌ ³ªÅ¸³­´Ù.
  • ectopic Cushing's syndrome
    À̼Ҽº Äí½Ì ÁõÈıº
  • Edinger-Westphal syndrome
    ¿¡µù°Å-¿þ½ºÆ®ÆÈ ÁõÈıº
  • effort syndrome
    ¿¡Æ÷Æ® ÁõÈıº
  • electrolyte deficiency syndrome
    ÀüÇØÁú °áÇÌ ÁõÈıº
  • empty sella syndrome
    °ø Å;îŰ¾È ÁõÈıº
    °¡Àå ÈçÇϰԴ ÁöÁÖ¸·ÀÌ Å;îŰ¾È Ⱦ°Ý¸·ÀÇ °á¼ÕºÎ¸¦ ÅëÇÏ¿© ºüÁ® µé¾î¿À´Â °ÍÀε¥ Çϼöü °æÀÌ Áö³ª´Â ±¸¸ÛÀÌ Å©´ÙµçÁö ¶Ç´Â ´Ù¸¥ °á¼ÕºÎ°¡ ÀÖ¾î ÀϾ´Ù. ³ú ô¼ö¾×¾ÐÀ¸·Î ÀÎÇØ Çϼöü°¡ À§ÃàµÇ°í Å;îŰ¾ÈÀº ºó ¸ð½ÀÀÌ µÈ´Ù. ´Ù¸¥ ¿øÀÎÀ¸·Î´Â Sheehan ÁõÈıº, ¼±Á¾ÀÇ ¿ÏÀü °æ»ö ÈÄ ¼¶À¯¼º ¹ÝÈçÈ­ ±×¸®°í ¼ö¼úÀ̳ª ¹æ»ç¼±Àû Çϼöü ÀýÁ¦ µîÀÌ´Ù. ´ë°³ ȯÀÚ´Â Çϼöü ºÎÀüÀ» ¹æÁöÇÒ ¸¸ÇÑ ÃæºÐÇÑ ½ÇÁúÀÌ º¸Á¸µÈ´Ù. ±×·¯³ª ¶§·Î´Â Ç⼺ È£¸£¸ó ÇÑ Á¾·ù ¶Ç´Â ±× ÀÌ»óÀÇ ºÐºñ ºÎÁ·ÀÌ ÀÖ´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 12
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)
Beradinelli's syndrome <syndrome> The clinical findings of accelerated growth, lipodystrophy with muscular hypertrophy, hepatomegaly and lipaemia.
(27 Sep 1997)
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