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"Hammer Toe Syndrome"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • Goodpasture¡¯s syndrome
    ±ÂÆÄ½ºÃ³ÁõÈıº
  • gray syndrome
    ȸ»öÁõÈıº
  • Guillain-Barre syndrome
    ±æ·©-¹Ù·¹ÁõÈıº
  • Ganser syndrome
    °£ÀúÁõÈıº
  • hypereosinophilic syndrome
    °ú´ÙÈ£»ê±¸ÁõÈıº
  • hyper-IgM syndrome
    °í¸é¿ª±Û·ÎºÒ¸°MÁõÈıº
  • hyperimmunoglobulin E syndrome
    °í¸é¿ª±Û·ÎºÒ¸°EÁõÈıº
  • hyperstimulation syndrome
    °ú´ÙÀÚ±ØÁõÈıº
  • hyperventilation syndrome
    °ú´Ùȯ±âÁõÈıº
  • hyperviscosity syndrome
    °ú´ÙÁ¡¼ºÁõÈıº
  • hypoventilation syndrome
    Àúȯ±âÁõÈıº
  • hemolytic uremic syndrome
    ¿ëÇ÷¿äµ¶ÁõÈıº
  • hemopleuropneumonic syndrome
    Ç÷¾×°¡½¿¸·Æó·ÅÁõÈıº, Ç÷¾×È丷Æó·ÅÁõÈıº
  • Hallervorden-Spatz syndrome
    ÇÒ·¯º¸¸£µ§-½´ÆÄÃ÷ÁõÈıº
  • hemorrhagic fever with renal syndrome
    ÃâÇ÷¿­ÄáÆÏÁõÈıº, ÃâÇ÷¿­½ÅÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
  • ¿µ¹®
    ÇѱÛ
  • gastrointestinal syndrome
    À§Àå°üÁõÈıº
  • general adaptation syndrome
    Àü½Å¼øÀÀÁõÈıº
  • green nail syndrome
    ³ì»ö¼Õ¹ßÅéÁõÈıº
  • hematopoietic syndrome
    Á¶Ç÷ÁõÈıº
  • hemolytic-uremic syndrome
    ¿ëÇ÷¿äµ¶ÁõÈıº
  • hemopleuropneumonic syndrome
    Ç÷¾×°¡½¿¸·ÇãÆÄÁõÈıº
  • hereditary adrenogenital syndrome
    À¯ÀüºÎ½Å¼º±âÁõÈıº
  • heredofamilial hypothalamohypophyseal syndrome
    À¯Àü°¡Á·½Ã»óÇϺγúÇϼöüÁõÈıº
  • hunger pain syndrome
    °øº¹ÅëÁõÈıº
  • hyperstimulation syndrome
    °ú´ÙÀÚ±ØÁõÈıº
  • hyperventilation syndrome
    °ú´ÙÈ£ÈíÁõÈıº
  • hyperviscosity syndrome
    °ú´ÙÁ¡¼ºÁõÈıº
  • hypoventilation syndrome
    È£ÈíÀúÇÏÁõÈıº
  • idiopathic cramp syndrome
    Ư¹ß°æ·ÃÁõÈıº
  • idiopathic respiratory distress syndrome
    Ư¹ßÈ£Èí°ï¶õÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
  • ¿µ¹®
    ÇѱÛ
  • HELLP syndrome
    HELLP ÁõÈıº
  • Hallerman Streiff syndrome
    ÇÒ·¯¸¸-½ºÆ®¶óÀÌÇÁÁõÈıº.
  • Hallzouns syndrome
    ȦÁ¸ÁõÈıº
  • Hamman Rich syndrome =diffuse interstitial pulmonary fibrosis
    ÇØ¸Õ- ¸®Ä¡ÁõÈıº.
  • Hamman-Rich syndrome
    ÇØ¸Õ-¸®Ä¡ ÁõÈıº
  • Heerfordts syndrome => uveoparotid fever
    Ç츣Æ÷¸£Æ® ÁõÈıº
  • Henoch Schoenlein syndrome
    Çì³ëÈ£-½¨¶óÀÎÁõÈıº.
  • Henoch Schoenlein syndrome
    Çì³ëÈ£-½¨¶óÀÎÁõÈıº
  • Hermansky-Pudlak syndrome
    Ç츣¸¸½ºÅ°-Ǫµé¶óÅ© ÁõÈıº
  • Hermansky-Pudlak syndrome => oculocutaneous albinism
    ¾È±¸ ÇǺΠ¹é»öÁõ
  • Hoffmann s syndrome
    È£ÇÁ¸¸ÁõÈıº.
  • Holt Oram syndrome
    ȦƮ-¿À¶÷ÁõÈıº.
  • Horners syndrome
    È£³Ê ÁõÈıº
  • Horners syndrome
    È£³Ê¾¾ ÁõÈıº
  • Horners syndrome
    È£¸£³ÊÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • 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)
  • arthritis-dermatitis syndrome
    °üÀý¿°-ÇǺο° ÁõÈıº
  • ashermans syndrome
    ¾Æ¼Å¸¸ ÁõÈıº
  • asphyctic syndrome
    Áú½ÄÁõÈıº.
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 9
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...
CBS cervicobrachial syndrome; chronic brain syndrome; clinical behavioral science; conjugated bile salts...
CHS central hypoventilation syndrome; Chediak-Higashi syndrome; cholinesterase; chondroitin sulfate; com...
CPS carbamoylphosphate synthetase; cardioplegic perfusion solution; centipoise; cervical pain syndrome; ...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 9
BMS Burning Mouth Syndrome
CFS Cancer Family Syndrome
CDGS Carbohydrate Deficient Glycoprotein Syndrome
CSS Carotid Sinus Syndrome
C.T.S. Carpal Tunnel Syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • 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
  • 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
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
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)
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)
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