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  • ¿µ¹®
    ÇѱÛ
  • Pancoast syndrome
    ÆÒÄÚ½ºÆ®ÁõÈıº
  • Pickwickian syndrome
    ÇÈÀ¨ÁõÈıº
  • Pierre Robin syndrome
    ÇÇ¿¡¸£·Î¹ðÁõÈıº
  • placental transfusion syndrome
    ŹݼöÇ÷ÁõÈıº
  • polycystic ovarian syndrome
    ´Ù³¶³­¼ÒÁõÈıº
  • postmenopausal syndrome
    Æó°æÈÄÁõÈıº
  • post-myocardial infarction syndrome
    ½É±Ù°æ»öÈÄÁõÈıº
  • postnasal drip syndrome
    ÄÚµÚÈ帧ÁõÈıº, Èĺñ·çÁõÈıº
  • postpericardiotomy syndrome
    ½É³¶¸·Àý°³¼úÈÄÁõÈıº
  • postpolio syndrome
    ¼Ò¾Æ¸¶ºñÈÄÁõÈıº
  • Prader-Willi syndrome
    ÇÁ·¡´õ-Àª¸®ÁõÈıº
  • premenstrual syndrome
    ¿ù°æÀüÁõÈıº
  • prune-belly syndrome
    ¸»¸°´ëÃß¹èÁõÈıº
  • pulmonary overinflation syndrome
    Æó°úµµÆØÃ¢ÁõÈıº
  • paraneoplastic syndrome
    ½Å»ý¹°µþ¸²ÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
  • ¿µ¹®
    ÇѱÛ
  • rubber jaw syndrome
    °í¹«ÅÎÁõÈıº
  • runting syndrome
    ¼Ò¸ðÁõÈıº
  • syndrome
    ÁõÈıº
  • syndrome of crocodile tears
    ¹Ì°¢´«¹°ÁõÈıº
  • scalded skin syndrome
    È­»óÇǺÎÁõÈıº
  • sensory syndrome
    °¨°¢ÁõÈıº
  • Sertoli-cell-only syndrome
    ¹öÆÀ¼¼Æ÷ÁõÈıº, ¼¼¸£Å丮¼¼Æ÷ÁõÈıº
  • shaken baby syndrome
    Èçµé¸°¾ÆÀÌÁõÈıº
  • shock syndrome
    Ãæ°ÝÁõÈıº
  • short bowel syndrome
    ÀÛÀºÃ¢ÀÚÁõÈıº
  • shoulder-hand syndrome
    ¾î±ú¼ÕÁõÈıº
  • sleep apnea syndrome
    ¼ö¸é¹«È£ÈíÁõÈıº
  • sleep choking syndrome
    ¼ö¸éÁú½ÄÁõÈıº
  • somatizing syndrome
    ½ÅüȭÁõÈıº
  • stasis syndrome
    âÀÚÁ¤Ã¼ÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
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    ÇѱÛ
  • Parinauds oculonoduler syndrome
    ÆÄ¸®³ë¾È ¸²ÇÁÀý ÁõÈıº.
  • Parinauds syndrome
    ÆÄ¸®³ëµåÁõÈıº
  • Peutz-Jeghers syndrome
    Ç»Ã÷Á¦°Å½ºÁõÈıº.
  • Peutz-Jeghers syndrome
    Æ÷ÀÌÃ÷-¿¹°ÅÁõÈıº.
  • Pickwickian syndrome
    ÇÇÅ©À§Å© ÁõÈıº
  • Plummer Vinson syndrome
    Ç÷¯¸Ó-ºó¼ÕÁõÈıº
  • Plummer-Vinson syndrome
    Ç÷¯¸Óºó½¼ÁõÈıº.
  • Poland syndrome
    Æú¶õµåÁõÈıº
  • Posner-Schlossman syndrome=>glaucomatocyclitic crisis
    Æ÷½º³Ê-½¯·Î½º¸¸ ÁõÈıº
  • Proteus syndrome
    ÇÁ·ÎÅ׿콺 ÁõÈıº
  • RDS=£¾respiratory distress syndrome
    È£Èí°ï¶õÁõÈıº.
  • Ramsey-Hunt syndrome
    ·¥Áö¡©Ç寮 ÁõÈıº
  • Raynaud s syndrome
    ·¹À̳ëÁõÈıº.
  • Refsums syndrome
    ·¾¼ûÁõÈıº
  • Reiter s syndrome
    ¶óÀÌÅÍÁõÈıº.
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
  • ¿µ¹®
    ÇѱÛ
  • 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
  • broad thumb-hallux syndrome
    ±¤¾öÁö¼Õ,¹ß°¡¶ôÁõÈıº
  • bronze baby syndrome
    ûµ¿»ö¾Æ±âÁõÈıº
  • bruising syndrome
    Ÿ¹Ú»óÁõÈıº.
  • budd-chiari syndrome
    ¹Ùµå-Ű¾Æ¸® ÁõÈıº (¡­ñøý¦ÏØ)
  • bulbar syndrome
    ¿¬¼öÁõÈıº(æÅâÐñøý¦ÏØ)
  • burning feet syndrome
    ÀÛ¿­°¢ÁõÈıº(¡­ñøý¦ÏØ), ¼ÒÀÛÁ·ÁõÈıº(áÀíÇðëñøý¦ÏØ).
  • camptomelic syndrome
    ±¼Áö ÁõÈıº.[¼Ò¾Æ]Áöü ±¼°î ÁõÈıº(ò¶ô÷ÏÝÍØñøý¦ÏØ) .
  • camptomelic syndrome
    ±¼ÁöÁõÈıº.¼Ò¾ÆÁöü±¼°îÁõÈıº(ò¶ô÷ÏÝÍØñøý¦ÏØ) .
  • capillary leak syndrome
    ¸ð¼¼Ç÷°ü´©ÃâÁõÈıº
  • caplans syndrome
    ijÀÌÇöõ ÁõÈıº (¡­ñøý¦ÏØ)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
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: 16
DHF/DSS Dengue Haemorrhagic Fever/Dengue Shock Syndrome
DSS Dengue Shock Syndrome
DDS Denys Drash syndrome
DGS Di George syndrome
DILS Diffuse Infiltrative Lymphocytosis Syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • infantile stiff skin syndrome
    ¿µ¾Æ ÇǺΠ°æÁ÷ ÁõÈıº
  • inspissated bile syndrome
    ³óÃà ´ãÁó ÁõÈıº
  • intermediate syndrome
    Áß°£Çü ÁõÈıº
  • iridocorneal-endothelial syndrome
    ȫä °¢¸· ³»ÇÇ ÁõÈıº
  • iris-nevus syndrome
    ȫä ¸ð¹Ý ÁõÈıº
  • irritation syndrome
    ÀÚ±Ø ÁõÈıº
  • jaw winking syndrome
    ÇÏ¾Ç À®Å© ÁõÈıº
  • jet lag syndrome
    ºñÇà ½ÃÂ÷ ÁõÈıº
  • Kast's syndrome
    Ä«½ºÆ® ÁõÈıº
    °ñ°ÝÀÇ ´Ù¹ß¼º ¿¬°ñÁ¾¿¡ ÇØ¸é»ó Ç÷°üÁ¾ÀÌ µû¸£´Â Áúº´.
  • Kearns-Sayre syndrome
    ÄÁ½º-¼¼À̾î ÁõÈıº
  • Kelly Paterson syndrome
    Ä̸®ÆäÅͽ¼ ÁõÈıº
  • kidney nephrotic syndrome
    ½Å ÁõÈıº
  • Kleinfelter syndrome
    Ŭ¶óÀÎÆçÅÍ ÁõÈıº
    1. 1942³â H.F. Ŭ¶óÀÎÆçÅͰ¡ ±âÀçÇÑ ¼º¿°»öü ÀÌ»ó ÁõÈıº. Á¤»óÀÎÀÇ ¼º¿°»öüÇüÀº ³²¼º XY, ¿©¼º XX¸¦ ³ªÅ¸³»Áö¸¸, ÀÌ ÁõÈıº¿¡¼­´Â ¼º¿°»öüÇüÀÌ XXY, XXYY, XXXXY µîÀÇ ¿©·¯ °¡Áö ÀÌ»óÇÑ ÇüŸ¦ ³ªÅ¸³½´Ù. ¿Ü¼º±â, ü°Ý, ¼ºÂ¡ µîÀÇ Æ¯Â¡ÀûÀÎ Áõ¼¼·Î º¼ ¶§¿¡ ¿ÏÀüÇÑ ³²¼ºÀÌ °áÈ¥ÇÏ¿© ¼º»ýȰ±îÁö ÇÏ¿´À¸³ª, ÀÚ½ÄÀÌ ¾øÀÚ ºÎºÎ°¡ ÇÔ²² º´¿øÀ» ã¾Æ°¡¼­ ¿°»öü¸¦ °Ë»çÇØ º¸°í ³²ÀÚ¿¡°Ô ÀÌ ÁõÈıºÀÌ ÀÖÀ½À» ¾Ë°Ô µÇ´Â °æ¿ì°¡ ¸¹´Ù. ÀÌ ¹Û¿¡ ¼ºÀÎÀÌ µÇ¾î ³ªÅ¸³ª´Â ÁÖ¿ä Áõ¼¼¸¦ µé¸é, ¼Ò°íȯ, ¿©¼ºÇü À¯¹æÁõ, ¹«Á¤ÀÚÁõ, ºÒÀÓ, ¿äÁß °í³ªµµÆ®·ÎÇÉ
  • Klippel Feil syndrome
    Ŭ¸®Æç ÆÄÀÏ ÁõÈıº, Ŭ¸®Æç-ÆäÀÏ ÁõÈıº
    °æÃß ¼öÀÇ °¨¼Ò ȤÀº ´Ù¹ß¼º ÆíÃø ôÃßÀÇ °ñ À¯ÇÕ¿¡ ±âÀÎÇÑ °æºÎÀÇ ´ÜÃà, °æºÎ ¿îµ¿ Àå¾Ö µîÀ» Ư¡À¸·Î ÇÏ´Â ÁõÈıº.
  • Korsakov syndrome
    ÄÚ¸£»çÄÚÇÁ ÁõÈıº
    ±â¾ï·ÂÀÇ Àå¾Ö, ½Ã°£Àû, °ø°£ÀûÀÎ ÁüÀÛÀÌ °ï¶õÇÑ ÁüÀÛ ÀǽÄÀÇ Àå¾Ö, °Ç¸Á, ÀÛ¾îÁõ µîÀÇ ¿©·¯ Áõ¼¼¸¦ ³ªÅ¸³»´Â ÁõÈıº. °Ç¸Á ÁõÈıºÀ̶ó°íµµ ÇÑ´Ù. ȯÀÚ´Â ½ÃÀÏÀ» Àؾî¹ö¸®°í Áö±Ý ¸· Áö³ª¿Â ±æµµ Àؾî¹ö¸®¸ç ±×³¯ÀÇ ½Ä»çÀÇ ³»¿ëÀ̳ª ¸éȸÀÚ µîµµ Àؾî¹ö¸®°í »ý°¢Çس»Áö ¸øÇÑ´Ù. ¶Ç ÁüÀÛ ÀǽÄÀÇ Àå¾Ö ¶§¹®¿¡ ÀڱⰡ ³õ¿© ÀÖ´Â ÇöÀçÀÇ »óȲµµ Á¤È®ÇÏ°Ô ÆÇ´ÜÇÏÁö ¸øÇÑ´Ù. Áú¹®¿¡ ´äÇÏ´Â ³»¿ëÀº °ø»óÀûÀ̰ųª ±× Àå¼ÒÀÇ Àڱؿ¡ ÃË¹ßµÇ¾î ¾Ö¸ÅÇÑ ¸»À» ÇÏ°Ô µÈ´Ù. ÀϹÝÀûÀ¸·Î Áö´É Àå¾Ö¸¦ ³ªÅ¸³»´Â ³ëÀμº Ä¡¸Å³ª ÁøÇึºñ ¿Ü¿¡, ¾ËÄÚ¿Ã Á¤½Åº´ µî¿¡¼­ º¼ ¼ö ÀÖÀ¸¸ç, µÎºÎ ¿Ü»óÀ̳ª ³ú Á¾¾ç µîÀÇ °æ¿ì¿¡µµ ³ªÅ¸³­´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
Vernet's syndrome <syndrome> A syndrome characterised by paralysis of the motor components of the glossopharyngeal, vagus, and accessory cranial nerves as they lie in the posterior fossa; it is most commonly the result of head injury.
(05 Mar 2000)
Maroteaux-Lamy syndrome <biochemistry, syndrome> An error of mucopolysaccharide metabolism due to deficiency of the lysosomal enzyme arylsulphatase B.
It is characterised by excretion of dermatan sulfate in the urine, growth retardation, lumbar kyphosis, sternal protrusion, genu valgum, usually hepatosplenomegaly, and no mental retardation.
Onset occurs after two years of age.
Inheritance: autosomal recessive.
Synonym: polydystrophic dwarfism, mucopolysaccharidosis type VI.
(05 Mar 2000)
Marshall syndrome <syndrome> Syndrome of mid-face hypoplasia, cataract, sensorineural hearing loss, and hypohidrosis. It is disputed whether this syndrome is distinct from Stickler's syndrome.
(05 Mar 2000)
carotid artery occlusive syndrome <syndrome> Aortic arch syndrome, also referred to by many as vertebral-basilar artery disease, carotid artery occlusive syndrome and subclavian steal syndrome.
Characterised by a constellation of signs and symptoms which occur secondary to abnormalities in the major arteries which extend off of the aortic arch. These abnormalities are structural and most often secondary to the effects of atherosclerosis, blood clots, trauma or a congenital abnormality.
Symptoms of this condition include various neurologic symptoms, reduction in pulse and changes in blood pressure.
(27 Sep 1997)
carotid sinus syndrome <syndrome> Stimulation of a hyperactive carotid sinus, causing a marked fall in blood pressure due to vasodilation, cardiac slowing, or both; syncope with or without convulsions or A-V block may occur.
Synonym: Charcot-Weiss-Baker syndrome.
(05 Mar 2000)
Martorell's syndrome <syndrome> Aortic arch syndrome, also referred to by many as vertebral-basilar artery disease, carotid artery occlusive syndrome and subclavian steal syndrome is characterised by a constellation of signs and symptoms which occur secondary to abnormalities in the major arteries which extend off of the aortic arch. These abnormalities are structural and most often secondary to the effects of atherosclerosis, blood clots, trauma or a congenital abnormality. Symptoms of this condition include various neurologic symptoms, reduction in pulse and changes in blood pressure.
(27 Sep 1997)
masa syndrome <syndrome> MASA stands for mental retardation, aphasia, shuffling gait, and adducted thumbs.
Features of the syndrome include (1) neurologically: mental retardation and aphasia (lack of speech); (2) limbs: adducted (clasped) thumbs, absent extensor pollicis longus and/or brevis muscles to the thumb, shuffling gait, and leg spasticity; (3) growth: small body size; (4) skeleton: lumbar lordosis (sway back).
It is inherited as an x-linked trait and so affects mainly boys. Alternative names for masa include clasped thumb and mental retardation, congenital clasped thumb with mental retardation, adducted thumb with mental retardation, and the gareis-mason syndrome.
inheritance: X-linked
(29 Dec 1998)
carpal tunnel syndrome <syndrome> A condition where there is a disturbance of median nerve function in the wrist as the nerve passes through the carpal tunnel.
A buildup of scar tissue (inside the carpal tunnel) can lead to this surgically correctable problem. Often treated with splinting and anti-inflammatory agents.
(27 Sep 1997)
Carpenter's syndrome <syndrome> The association of primary hypothyroidism, primary adrenocortical insufficiency, and diabetes mellitus.
Origin: C. C. J. Carpenter
Synonym: acrocephalopolysyndactyly.
Origin: G. Carpenter
(05 Mar 2000)
vertical retraction syndrome <syndrome> A retraction of the globe and pseudoptosis on attempted adduction; due to co-innervation of the horizontal recti. Sometimes there is an inability to abduct the affected eye (type 1), or adduct the affected eye (type 2), or both (type 3).
Synonym: Duane's syndrome.
(05 Mar 2000)
Gerstmann-Straussler-Scheinker syndrome <syndrome> A familial spongiform encephalopathy. Transgenic mice with a mutant form of the PrP gene from patients with this syndrome develop degenerative brain disease that is similar, but not identical, to that caused by scrapie.
It is a more chronic cerebellar form of spongiform encephalopathy, producing a neurodegenerative condition that has morphological similarities to Creutzfeldt-Jakob syndrome. However, in this syndrome there is slower progression, signs of spinocerebellar ataxia, and the spongiosis is less pronounced.
Prion proteins and amyloid plaques are found in the brain of patients with the syndrome. A germline mutation of the prion protein has been demonstrated.
(12 Jul 2000)
Gerstmann syndrome <syndrome> Tetrad of finger agnosia, dysgraphia or agraphia, dyscalculia or acalculia, and right-left disorientation producing confusion of laterality of the body.
The syndrome can occur in brain-damaged and apparently normal children as well as in adults who have had vascular accidents, and is caused by lesions between the occipital area and the angular gyrus.
(12 Jul 2000)
Parinaud's oculoglandular syndrome <syndrome> Unilateral conjunctival granuloma with preauricular adenopathy in tularaemia, chancre, and tuberculosis.
(05 Mar 2000)
Parinaud's syndrome <syndrome> Paralysis of conjugate upward gaze with a lesion at the level of the superior colliculi; Bell's phenomenon is present.
Synonym: Parinaud's ophthalmoplegia.
(05 Mar 2000)
parinaud syndrome <radiology> Paralysis of upward gaze, also known as: supranuclear palsy, compression of tectal (quadrigeminal) plate, by pineal mass
(12 Dec 1998)
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