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"general adaptation 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
  • gay bowel syndrome
    µ¿¼º¾ÖÀÚâÀÚÁõÈıº
  • 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
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  • ¿µ¹®
    ÇѱÛ
  • fish-odor syndrome
    ¹°°í±âÇâÁõÈıº
  • floppy infant syndrome
    Àú±äÀ徯ÁõÈıº, ±äÀåÀúÇÏ¿µ¾ÆÁõÈıº
  • fragile X syndrome
    À¯¾à¿¢½ºÁõÈıº
  • gastrointestinal syndrome
    À§Àå°üÁõÈıº
  • 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
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 10
  • ¿µ¹®
    ÇѱÛ
  • Ganser syndrome
    °µ¼­ÁõÈıº.
  • Gardner s syndrome
    °¡¾Æµå³ÊÁõÈıº.
  • Gianotti-Crosti syndrome => infantile papular acrodermatitis
    Àð³ëƼ Å©·Î½ºÆ¼ ÁõÈıº
  • Gilberts syndrome
    Áúº£¸£ÁõÈıº
  • Glucose-galactose malabsorption syndrome
    ±Û·çÄÚ¿À½º-°¥¶ôÅ佺Èí¼öÀå¾ÖÁõÈıº(ýåâ¥î¡äôñøý¦ÏØ)
  • Goldenhars syndrome->oculo-auriculo-vertebral dysplasia
    °ñµçÇÏÁõÈıº
  • Goltzs syndrome => focal dermal hypoplasia
    ±¹¼Ò ÁøÇÇ Çü¼ººÎÀüÁõ
  • Golzs syndrome
    °ñÁî ÁõÈıº
  • Goodpasture s syndrome
    ±¸µåÆÐ½ºÃò¾î ÁõÈıº.
  • Gradenigos syndrome
    Ãßü(÷ºÎ)¿° ÁõÈıº, ±×¶óµ¥´Ï
  • Graham-Little syndrome
    ±×·¹À̾ö ¸®Æ² ÁõÈıº
  • Grey platelet syndrome
    ±×·¹ÀÌÇ÷¼ÒÆÇÁõÈıº
  • Guillain Barre syndrome
    ±æ¶û-¹Ù·¹ ÁõÈıº.
  • Guillain-Barre syndrome
    ±æ¶û-¹Ù·¹ ÁõÈıº
  • HELLP syndrome
    HELLP ÁõÈıº
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  • ¿µ¹®
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  • 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.
  • atomic bomb syndrome
    ¿ø(ÀÚ)Æø(ź)ÁõÈıº.
  • atypical or mixed organic brain syndrome
    ºñÁ¤Çü ³»Áö È¥ÇÕÇü ±âÁú¼º ³úÁõÈıº
  • atypical schizophrenic syndrome
    ºñÁ¤Çü Á¤½ÅºÐ¿­¼º ÁõÈıº
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SSS scalded skin syndrome; secondary Sjogren syndrome; sick sinus syndrome; specific soluble substance; ...
TS Takayasu syndrome; Tay-Sachs; temperature sensitivity; temperature, skin; temporal stem; tensile str...
GHQ General Health Questionaire
GS   1) Gall Stone
  2) General Surgery
AAGP American Academy of General Practice; American Association for Geriatric Psychiatry
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AGS Adrenogenital Syndrome
AGS Alagille syndrome
AWS Alcohol Withdrawal Syndrome
AS Alport syndrome
ABS Amniotic Band Syndrome
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • 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
  • Devies syndrome
    µ¥ºò ÁõÈıº
  • Di George's syndrome
    µð, ÁÒ¿ÀÁö ÁõÈıº
    1. Èä¼±ÀÌ Çü¼ºµÇÁö ¸øÇÏ´Â Èä¼± ¹«Çü¼ºÁõÀ» µ¿¹ÝÇϹǷΠÀÎÇØ ¹ß»ýÇÏ´Â ¼¼Æ÷ ¸Å°³¼º ¸é¿ªÀÇ °áÇÌÀÌ ³ªÅ¸³ª´Â Áúº´. 2. Èä¼±ÀÇ ¹«Çü¼º ³»Áö ÀúÇü¼º°ú ¼±Ãµ¼º ½ÉÁúȯ. ºÎ°©»ó¼± ÀÌ»óÁõÀ» ¼ö¹Ý½ÃŰ´Â ¼±Ãµ¼º ¼¼Æ÷¼º ¸é¿ª ºÎÀü ÁõÈıºÀÌ¸ç ¸· ž ¶§¿¡ º¼ ¼ö ÀÖ´Â À̰³ÀÇ ÀúÀ§, ¾î»ó±¸ ¾ç¾ÈÀÇ °Ý¸® µîÀÇ Æ¯À¯ ¾È¸ð¿Í ºÎ°©»ó¼± ±â´É Å»¶ô¿¡ ÀÇÇÑ Àú Ä®½· Ç÷Áõ, ¿ïÇ÷¼º ½ÉºÎÀü µî¿¡ ÀÇÇÏ¿© ÀǽÉÀ» °¡Áö°Ô µÇ°í Èä¼± ¹× T¼¼Æ÷ ±â´ÉÀÇ °Ë»öÀ¸·Îµµ Áø´ÜÀÌ ³»·ÁÁø´Ù. º´ÀÎÀ¸·Î¼­´Â ÀÌ»óÁ¦±â°ü »çÀÌÀÇ °ü·Ã¿¡¼­ Å»ý 12ÁÖ °æÀÇ ¹ß»ý ÀÌ»óÀ» »ý°¢ÇÒ ¼ö ÀÖ´Ù.
  • diencephalic-hypophysial syndrome
    °£³ú Çϼöü ÁõÈıº
    ¿äºØÁõ, Áö¹æÁõ, ¼º±â À§Ãà, ½Ã¸óÁ µîÀÇ ÃÑĪ. °£³ú, ƯÈ÷ ½Ã»ó ÇϺο¡´Â ¿©·¯ °¡Áö ÀÚÀ²½Å°æ ÁßÃß°¡ Àִµ¥, °£³ú ÇϼöüÀÇ ¿¬°áÀº ÇØºÎÇлóÀ¸·Î³ª ±â´É»óÀ¸·Îµµ ±ØÈ÷ ¹ÐÁ¢ÇÑ °ü°è°¡ ÀÖ´Â °ÍÀÌ ¸í¹éÇØÁ®¼­, Áö±Ý±îÁö ³úÇϼöü°èÀÇ Àå¾Ö·Î ¸»¹Ì¾Ï¾Æ »ý±ä´Ù°í »ý°¢µÇ¾î¿Â À§À庴 µîÀÇ Áõ¼¼´Â °£³ú ÁßÃßÀÇ Àå¾Ö¸¸À¸·Î »ý±ä´Ù´Â °ÍÀÌ ¹àÇôÁ³´Ù.
  • diffuse hemorrhagic syndrome
    ¹Ì¸¸¼º ÃâÇ÷¼º ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 10
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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