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  • ¿µ¹®
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  • lymphoproliferative syndrome
    ¸²ÇÁ¼¼Æ÷Áõ½ÄÁõÈıº
  • middle lobe syndrome
    Áß°£¿±ÁõÈıº
  • milk-alkali syndrome
    ¿ìÀ¯¾ËÄ®¸®ÁõÈıº
  • morning glory syndrome
    ³ªÆÈ²ÉÁõÈıº
  • motor syndrome
    ¿îµ¿(ÁßÃß)ÁõÈıº
  • mucocutaneous lymph node syndrome
    Á¡¾×ÇǺθ²ÇÁÀýÁõÈıº
  • myasthenic syndrome
    ±Ù(À°)¹«·ÂÁõÈıº
  • Mallory-Weiss syndrome
    ¸»·Î¸®-¹ÙÀ̽ºÁõÈıº
  • myelodysplastic syndrome
    °ñ¼öÇü¼ºÀÌ»óÁõÈıº
  • myeloproliferative syndrome
    °ñ¼öÁõ½ÄÁõÈıº
  • myofascial pain syndrome
    ±Ù¸·ÅëÁõÁõÈıº
  • myofascial pain-dysfunction syndrome
    ±Ù¸·ÅëÁõ±â´ÉÀå¾ÖÁõÈıº
  • Marfan syndrome
    ¸¶¸£ÆÎÁõÈıº
  • maternal deprivation syndrome
    ¸ð¼º¹ÚÅ»ÁõÈıº
  • McCune-Albright syndrome
    ¸ÆÄï-¿Ãºê¶óÀÌÆ®ÁõÈıº
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  • neurovisceral syndrome
    ½Å°æ³»ÀåÁõÈıº
  • nutritional deficiency syndrome
    ¿µ¾ç°áÇÌÁõÈıº
  • obstructive sleep apnea syndrome
    Æó¼â¼ö¸é¹«È£ÈíÁõÈıº
  • oculoauriculovertebral syndrome
    ´«±Ó¹ÙÄûôÃßÁõÈıº
  • oral-facial-digital syndrome
    ÀÔ¾ó±¼¼Õ°¡¶ôÁõÈıº, ±¸°­¾È¸é¼öÁ·ÁöÁõÈıº
  • orbital apex syndrome
    ´«È®²ÀÁöÁõÈıº
  • organic brain syndrome
    ±âÁú³úÁõÈıº
  • organic mental syndrome
    ±âÁúÁ¤½ÅÁõÈıº
  • otocraniocephalic syndrome
    ±Í¸Ó¸®ÁõÈıº, À̵ΰ³ÁõÈıº
  • overlap syndrome
    °ãħÁõÈıº, ÁßøÁõÈıº
  • overwear syndrome
    °úµµÂø¿ëÁõÈıº
  • preleukemia myelodysplastic syndrome
    °ñ¼öÇü¼ºÀÌ»óÁõÈıº
  • pancoast syndrome
    ÆÇÄÚ½ºÆ®ÁõÈıº
  • peeling skin syndrome
    ÇǺιڸ®ÁõÈıº
  • phantom lover syndrome
    ȯ»ó¿¬ÀÎÁõÈıº
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  • Menkes (kinky) hair syndrome
    ¸àÄɾûÅ´ÅÐ ÁõÈıº
  • Menkes kinky hair syndrome
    ¸àÄÉŲ۸ðÁõÈıº
  • 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)
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  • blind loop syndrome
    ¸ÍÀå°ü ÁõÈıº(Øîíóηñøý¦ÏØ)
  • blind spot syndrome
    ¸ÍÁ¡ÁõÈıº(ØîïÇñøý¦ÏØ).
  • blooms syndrome
    ºí·ç¿ò ÁõÈıº (¡­ñøý¦ÏØ)
  • blue rubber-bleb nevus syndrome
    û»ö°í¹«¼öÆ÷¸ð¹ÝÁõÈıº
  • blue rubber-bleb nevus syndrome
    û»ö°í¹«¼öÆ÷¸ð¹ÝÁõÈıº(ôìßä¡­â©øÜÙ½Úèñøý¦ÏØ)
  • borderline syndrome
    °æ°è¼º ÁõÈıº
  • bradycardia tachycardia syndrome
    ¼­ºó¸Æ ÁõÈıº(ßïÞµØæ ñøý¥ÏØ).
  • bradycardia tachycardia syndrome
    ¼øÈ¯¼­¸Æºó¸ÆÁõÈıº.
  • bradytachycardia syndrome
    ¼­ºó¸ÆÁõÈıº(ßïÞºØæñøý¦ÏØ).
  • brain death syndrome
    ³ú»çÁõÈıº(ÒàÞÝñøý¦ÏØ).
  • brain stem syndrome
    ³ú°£ÁõÈıº(¡­ñøý¦ÏØ).
  • brain syndrome
    ³úÁõÈıº
  • brain syndrome, acute, chronic
    ±Þ¼º, ¸¸¼º ³úÁõÈıº.
  • breast/ovarian familial cancer syndrome
    À¯¹æ/³­¼Ò °¡Á·¼º ¾ÏÁõÈıº
  • brittle hair syndrome
    Ãë¾à¸ð¹ßÁõÈıº
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LDUB long double upright brace
LE lactate extraction; left ear; left eye; leukocyte elastase; leukoerythrogenic; live embryo; Long Eva...
LLB left lateral border; long-leg brace
LLC Lewis lung carcinoma; liquid-liquid chromatography; long-leg cast; lymphocytic leukemia
LLCC long-leg cylinder cast
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VLCAD Very long chain acyl-CoA dehydrogenase
VLCAD Very long chain acyl-coenzyme A dehydrogenase
VLCFA Very long chain fatty acid
L.A. long acting
LCT long chain
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  • 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.
  • encephalitis syndrome
    ³ú¿° ÁõÈıº
  • encephalotrigeminal syndrome
    ³ú »ïÂ÷ ½Å°æ ÁõÈıº
  • eosinophilia myalgia syndrome
    È£»ê±¸¼º ±ÙÀ°Åë ÁõÈıº, È£»ê±¸ Áõ´Ù¼º ±ÙÀ°Åë ÁõÈıº
  • eosinophilic pulmonary syndrome
    È£»ê¼º Æó ÁõÈıº
    ¸¸¼º È£»ê±¸¼º Æó·ÅÀº ÆóÆ÷ ¼¼Ã´À̳ª »ý°Ë»ó È£»ê±¸°¡ Æó Á¶Á÷ÀÇ ¸»Ãʺο¡ Ä§ÂøµÈ ¼Ò°ßÀ» Ư¡À¸·Î ÇÏ´Â ÁõÈıºÀ» ÀǹÌÇÑ´Ù. Ç÷¾× È£»ê±¸ Áõ°¡°¡ ´ëºÎºÐ °üÂûµÈ´Ù. ¸¸¼º È£»ê±¸¼º Æó·ÅÀº ÁÖ·Î ¿©ÀÚ¿¡ ³ªÅ¸³ª¸ç, ¹ß¿­, ¹ßÇÑ, üÁß °¨¼Ò, È£Èí °ï¶õÀÌ Æ¯Â¡ÀÌ´Ù. Ä¡·á´Â °æ±¸
  • epidermal nevus syndrome
    Ç¥ÇÇ ¸ð¹Ý ÁõÈıº
  • excited skin syndrome
    ÈïºÐ¼º ÇǺΠÁõÈıº
  • extrapyramidal syndrome
    Ãßü¿Ü·Î ÁõÈıº
  • facio-auriculo-vertebral syndrome
    ¾È¸é-ÀÌ-ôÃß ÁõÈıº
  • Fanconi's syndrome
    Fanconi ÁõÈıº
    1. Ç÷±¸°¨¼ÒÁõ, °ñ¼öÀÇ Çü¼º ºÎÀü, ¸á¶ó´Ñ Ä§Âø¿¡ ÀÇÇÑ ÇǺÎÀÇ »ö¼Ò¹Ý, ±Ù°ñ°Ý°è¿Í ºñ´¢ »ý½Ä°èÀÇ ¼±Ãµ¼º ÀÌ»óÀ» Ư¡À¸·Î ÇÏ´Â À¯Àü¼º Áúȯ. 2. ±ÙÀ§ ¼¼´¢°üÀÇ ±â´ÉÀå¾Ö·Î ÀÎÇÑ ÀÏ·ÃÀÇ ÁúȯÀ» °¡¸£Å°´Â ¿ë¾î. °íÀλ괢, ´ç´¢, Àü¾Æ¹Ì³ë»ê´¢, Áßź»ê¿°°ú ¼öºÐÀÇ ¼Õ½ÇÀÌ 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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