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"hyperactive child 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
  • Reiter¡¯s syndrome
    ¶óÀÌÅÍÁõÈıº
  • respiratory distress syndrome
    È£Èí°ï¶õÁõÈıº
  • radicular syndrome
    ½Å°æ»Ñ¸®ÁõÈıº, ½Å°æ±ÙÁõÈıº
  • retraction syndrome
    ¾È±¸ÈÄÅðÁõÈıº
  • scalded skin syndrome
    È­»óÇǺÎÁõÈıº
  • staphylococcal scalded skin syndrome
    Æ÷µµ¾Ë±Õ¼º¿­»óÇǺÎÁõÈıº, Æ÷µµ±¸±Õ¼º¿­»óÇǺÎÁõÈıº
  • stasis syndrome
    âÀÚÁ¤Ã¼ÁõÈıº, ÀåÁ¤Ã¼ÁõÈıº
  • Steele-Richardson-Olszewski syndrome
    ½ºÆ¿-¸®Ã³µå½¼-¿Ã½ºÁ¦ºê½ºÅ°ÁõÈıº
  • Scheie syndrome
    »þÀÌ¿¡ÁõÈıº
  • Stevens-Johnson syndrome
    ½ºÆ¼ºì½º-Á¸½¼ÁõÈıº
  • stiff-man syndrome
    °­Á÷ÁõÈıº
  • streptococcal toxic shock syndrome
    »ç½½¾Ë±Õµ¶¼º¼îÅ©ÁõÈıº, ¿¬¼â±¸±Õµ¶¼º¼îÅ©ÁõÈıº
  • sudden infant death syndrome
    ¿µ¾Æµ¹¿¬»çÁõÈıº
  • superior mesenteric artery syndrome
    À§Ã¢ÀÚ°£¸·µ¿¸ÆÁõÈıº, À§Àå°£¸·µ¿¸ÆÁõÈıº
  • superior orbital fissure syndrome
    À§´«È®Æ´»õÁõÈıº, »ó¾È¿Í¿­ÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • thalamic syndrome
    ½Ã»óÁõÈıÙ
  • time zone change syndrome
    (¢¡jet lag syndrome) ºñÇà½ÃÂ÷ÁõÈıº
  • toxic shock syndrome
    µ¶¼ÒÃæ°ÝÁõÈıº
  • transurethral resection syndrome
    °æ¿äµµÀýÁ¦ÈÄÁõÈıº
  • trisomy 18 syndrome
    18¼¼¿°»öüÁõÈıº
  • ulnar tunnel syndrome
    ÀÚ»À±¼ÁõÈıº, ô°ñ°üÁõÈıº
  • unknown genesis syndrome
    ¹ß»ý¹Ì»óÁõÈıº
  • vanishing testes syndrome
    °íȯ¼Ò¸êÁõÈıº
  • velocardiofacial syndrome
    ÀÔõÀå½ÉÀå¾ó±¼ÁõÈıº
  • virilizing syndrome
    ³²¼ºÈ­ÁõÈıº
  • vitreouswick wick syndrome
    À¯¸®Ã¼½ÉÁöÁõÈıº
  • wasting syndrome
    ¼Ò¸ðÁõÈıº
  • withdrawal syndrome
    ±Ý´ÜÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • Waardenburgs syndrome
    ¹Ù¸£µ§ºÎ¸£Å© ÁõÈıº
  • Wallenbergs syndrome
    ¹ß·»º£¸£Å©ÁõÈıº.
  • Waterhouse Friderichsen syndrome
    ¿ö¾îÅÍÇϿ콺-ÇÁ¸®µ¥¸®Å©¼¾ÁõÈıº.
  • Waterhouse-Friderichsen syndrome
    ¿öÅÍÇϿ콺-ÇÁ¸®µ¥¸¯¼¾ ÁõÈıº
  • Weber syndrome
    ¿þ¹öÁõÈıº
  • Weber-Cocayne syndrome
    ¿þ¹ö ÄÚÄÉÀÎ ÁõÈıº
  • Webers syndrome
    ¿þ¹öÁõÈıº.
  • Werners syndrome
    º£¸£³ÊÁõÈıº.
  • Wernicke Korsakoff syndrome
    º£¸£´ÏÄÉ-ÄÚ¸£»çÄÚÇÁÁõÈıº.
  • Wiskott-Aldrich syndrome
    ºñ½ºÄÚÆ®-¿Ãµå¸®Ä¡ ÁõÈıº
  • Wiskott-Aldrich syndrome
    À§½ºÄÚÆ® ¿Ãµå¸®È÷ ÁõÈıº
  • Wolff-Parkinson-White syndrome
    ¿ùÇÁÆÄŲ½¼È­ÀÌÆ® ÁõÈıº
  • Wyburn-Mason syndrome
    À§¹ø¸Å½¼ ÁõÈıº
  • X-linked lymphoproliferative syndrome
    ¼º¿°»öü ¿¬°ü ¸²ÇÁÁõ½Ä ÁõÈıº
  • XXY syndrome
    XXYÁõÈıº.
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  • ¿µ¹®
    ÇѱÛ
  • cord compression syndrome
    ô¼ö¾Ð¹ÚÁõÈıº(ô±âÐäâÚÞñøý¦ÏØ).
  • corporal leakage syndrome
    (ÇØ¸éü)´©Ãâ ÁõÈıº
  • corpus callosum syndrome
    ³ú·®ÁõÈıº(ÒàåÄñøý¦ÏØ).
  • corpus striatum syndrome
    ¼±Á¶Ã¼ÁõÈıº(¡­ñøý¦ÏØ).
  • costochondral syndrome
    ´Á¿¬°ñÁõÈıº(¡­ñøý¦ÏØ).
  • costoclavicular syndrome
    ´Á¼â°ñÁõÈıº(×ÎáðÍéñøý¦ÏØ).
  • cranial nerve syndrome
    ³ú½Å°æÁõÈıº(ÒàãêÌèñøý¦ÏØ).
  • crest syndrome
    CREST ÁõÈıº (¡­ñøý¦ÏØ)
  • cri du chat syndrome
    Å©¸®µÎ»þ ÁõÈıº(¡­ñøý¦ÏØ)
  • crigler-najjar syndrome
    Å©¸®±Û·¯³ª¾ßÁõÈıº(¡­ñøý¦ÏØ)
  • crocodile tears syndrome = gustatory lacrimation
    ¹Ì°¢´«¹° ÁõÈıº
  • culture-bound syndrome
    ¹®È­±Ç ÁõÈıº(ÙþûùÏêñøý¦ÏØ)
  • cystic duct syndrome
    ´ã³¶°üÁõÈıº(¡­ñøý¦ÏØ).
  • cystic duct syndrome
    ´ã³¶°üÁõÈıº(¡­ÁõÈıº).
  • dandy-walker syndrome
    ´íµð¿öÄ¿ ÁõÈıº (¡­ñøý¦ÏØ)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
SCAN suspected child abuse and neglect; systolic coronary artery narrowing
TBLC term birth, living child
wh ch wheel chair; white child
YLC youngest living child
ECG Electro-Cardio-Graphy(-Gram); ½ÉÀüµµ
   = EKG
  1. Conducting System Structu...
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CCHS Congenital central hypoventilation syndrome
CS Cowden syndrome
CS Cushing syndrome
CVS Cyclic vomiting syndrome
DSS Dejerine-Sottas Syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • 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.
  • Lacrimo-auriculo-dento-digital syndrome
    ´«¹° °ü ±Ó¹ÙÄû ÀÌ ¼Õ¹ß°¡¶ô ÁõÈıº
  • lacunar syndrome
    ¼Ò°ø¼º °æ»ö ÁõÈıº
  • Lafora syndrome
    ¶óÆ÷¶ó ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
Gardner-Diamond syndrome <syndrome> A condition, usually occurring in women, in which the individual bruises easily (purpura simplex) and the ecchymoses tend to enlarge and involve adjacent tissues, resulting in pain in the affected parts; so-called because similar lesions are produced by inoculation of the individual's blood or various components of red blood cells and it is thought to be a form of localised autosensitization, although no specific antibodies have been demonstrable; in some individuals, there seems to be a psychogenic mechanism.
Synonym: Gardner-Diamond syndrome, psychogenic purpura.
(05 Mar 2000)
Gardner's syndrome <syndrome> Multiple polyposis predisposing to carcinoma of the colon; also multiple tumours, osteomas of the skull, epidermoid cysts, and fibromas; autosomal dominant inheritance.
(05 Mar 2000)
gardner syndrome <radiology> Autosomal dominant, adenomas leading to colon carcinoma (treatment: colectomy), periampullary carcinoma, soft-tissue lesions, sebaceous cysts, subcutaneous fibromas, leiomyomas, lipomas, bony lesions, osteomas (especially in sinuses), exostoses, cortical thickening, dental abnormalities (caries, extra teeth, odontomas) see: polyposis syndromes
(12 Dec 1998)
gareis-mason syndrome <syndrome> An inherited (genetic) syndrome with characteristic features including (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). The syndrome is inherited as an X-linked trait and so affects mainly boys. Alternative names include MASA syndrome (MASA stands for mental retardation, aphasia, shuffling gait, and adducted thumbs), clasped thumb and mental retardation, congenital clasped thumb with mental retardation, and adducted thumb with mental retardation.
(12 Dec 1998)
malabsorption syndrome <syndrome> A variety of conditions in which digestion and absorption in the small intestine are impaired. Multiple causes including lymphoma, amyloid and other infiltrations, Crohn's disease, gluten sensitive enteropathy and the sprue syndrome in which the villi atrophy for unknown reasons.
(18 Nov 1997)
vasculocardiac syndrome of hyperserotonaemia An obsolete term for carcinoid syndrome.
(05 Mar 2000)
pancoast's syndrome <syndrome> Destructive lesions of the thoracic inlet with involvement of the brachial and sympathetic plexus or carcinoma of the lung apex. It is characterised by pain in the shoulder region radiating toward the axilla and scapula, sensory and motor disorders and wasting of the muscles of the hand, the bernard-horner syndrome, and compression of the blood vessels with oedema.
(12 Dec 1998)
Pancoast syndrome <syndrome> Lower trunk brachial plexopathy and Horner syndrome due to malignant tumour in the region of the superior pulmonary sulcus.
(05 Mar 2000)
vasovagal syndrome gowers' syndrome
vater syndrome <radiology> V vertebral anomalies vascular anomalies, A anal atresia, T tracheo-oesophageal fistula, E oesophageal atresia, R renal anomalies radial dysplasia
(12 Dec 1998)
Ramsay Hunt's syndrome <syndrome> An intention tremor beginning in one extremity, gradually increasing in intensity, and subsequently involving other parts of the body.
Synonym: progressive cerebellar tremor.
Facial paralysis, otalgia, and herpes zoster resulting from viral infection of the seventh cranial nerve and geniculate ganglion, a form of juvenile paralysis agitans associated with primary atrophy of the pallidal system.
Synonym: paleostriatal syndrome, pallidal syndrome.
Synonym: Ramsay Hunt's syndrome.
(05 Mar 2000)
gastrocardiac syndrome <syndrome> Disturbances of the heart's action due to faulty action of the digestive system, especially of the stomach.
(05 Mar 2000)
malignant carcinoid syndrome <syndrome> A symptom complex associated with carcinoid tumour and characterised by attacks of severe flushing of the skin, diarrhoeal watery stools, bronchoconstriction, sudden drops in blood pressure, oedema, and ascites. The carcinoid tumours are usually located in the gastrointestinal tract and metastasize to the liver. Symptoms are caused by tumour secretion of serotonin, prostaglandins, and other biologically active substances. Cardiac manifestations constitute carcinoid heart disease.
(12 Dec 1998)
malignant mole syndrome <syndrome> Irregularly shaped, variously coloured, distinctively melanocytic, 5 to 10 mm nevi occurring in large numbers (to over 100) primarily on the trunk and extremities, with a high risk of malignancy reported in several members and three generations of a family.
(05 Mar 2000)
gastrojejunal loop obstruction syndrome <syndrome> A complication of gastrojejunostomy, caused by acute or chronic obstruction of the afferent loop due to hernia, intussusception, kinking, volvulus, etc. It is characterised by pain and vomiting of bile-stained fluid and includes acute afferent loop obstruction and bilious vomiting.
(12 Dec 1998)
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