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  • ¿µ¹®
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  • 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
  • superior vena cava syndrome
    À§´ëÁ¤¸ÆÁõÈıº, »ó´ëÁ¤¸ÆÁõÈıº
  • supine hypotensive syndrome
    ´©¿îÀÚ¼¼ÀúÇ÷¾ÐÁõÈıº, ¾Ó¿ÍÀ§ÀúÇ÷¾ÐÁõÈıº
  • syndrome
    ÁõÈıº
  • syndrome of crocodile tears
    ¾Ç¾î´«¹°ÁõÈıº
  • syndrome of inappropriate antidiuretic hormone
    Ç×ÀÌ´¢È£¸£¸óºÎÀûÀýºÐºñÁõÈıº
  • syndrome of inappropriate antidiuretic hormone secretion
    Ç×ÀÌ´¢È£¸£¸óºÎÀûÀýºÐºñÁõÈıº
  • syndrome of inappropriate secretion of antidiuretic hormone
    Ç×ÀÌ´¢È£¸£¸óºÎÀûÀýºÐºñÁõÈıº
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    ÇѱÛ
  • 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
  • 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.
  • XXYY syndrome
    XXYYÁõÈıº.
  • Zieves syndrome
    ÁöºêÁõÈıº
  • Zollinger-Ellison syndrome
    Á¹¸µ°Å ¿¤¸®¼Õ ÁõÈıº
  • Zollinger-Ellison syndrome
    Á¹¸°°Å-¿¤¸®½¼ ÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • cold agglutinin syndrome
    ÇÑ·© ÀÀÁý¼Ò ÁõÈıº
  • cold agglutinin syndrome
    ÇÑ·©ÀÀÁý¼ÒÁõÈıº
  • cold hemolysin syndrome
    ÇÑ·© ¿ëÇ÷¼Ò ÁõÈıº
  • combined immunity deficiency syndrome
    º¹Çո鿪°áÇÌÁõÈıº.
  • combined immunodeficiency syndrome
    º¹ÇÕÇü ¸é¿ª°áÇÌ ÁõÈıº
  • combined immunodeficiency syndrome
    º¹ÇÕÇü¸é¿ª°áÇÌÁõ(Èıº)
  • concentration camp syndrome
    ¼ö¿ë¼Ò ÁõÈıº(â¥é»á¶ ñøý¦ÏØ)
  • congenital Q-T syndrome
    ¼±Ãµ¼º(à»ô¸àõ) QT ÁõÈıº.
  • congenital central hypoventilation syndrome
    ¼±Ãµ¼º ÁßÃß¼º °ú¼Òȯ±â ÁõÈıº(à»ô¸àõñéõÒàõΦá´üµÑ¨ñøý¦ÏØ)
  • congenital fibrosis syndrome
    ¼±Ãµ¼¶À¯ÁõÁõÈıº
  • congenital immunodeficiency syndrome
    ¼±Ãµ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • congenital immunodeficiency syndrome
    ¼±Ãµ¼º¸é¿ª°áÇÌÁõ(Èıº)
  • congenital rubella syndrome
    ¼±Ãµ¼ºÇ³Áø ÁõÈıº
  • congenital rubella syndrome
    ¼±Ãµ¼º dzÁøÁõÈıº(¡­ù¦òÖñøý¦ÏØ).
  • congenital rubella syndrome
    ¼±Ãµ¼ºÇ³ÁøÁõ(Èıº)
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SISS Sentinel Injury Surveillance System [for Gunshot and Stab Wounds] small inducible secreted substance...
SLL small lymphocytic lymphoma
sm an small animal
SMBFT small bowel follow-through
SMI Self-Motivation Inventory; senior medical investigator; severe mental impairment; silent myocardial ...
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SCUC small cell undifferentiated carcinoma
SGA small for gestational age infant
SGC small granule-containing
SH small hydrophobic
snoRNP small nucleolar ribonucleoprotein
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  • ¿µ¹®
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    ¼³¸í
  • 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
  • Lambert-Eaton myasthenic syndrome
    ¶÷¹öÆ®-ÀÌÆ° ±Ù¹«·ÂÁõ ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
Caffey-Silverman syndrome Neonatal subperiosteal bone formation over many bones, especially the mandible and clavicles and the shafts of long bones; it follows fever, usually appearing before 6 months of age and disappearing during childhood.
Synonym: Caffey's disease, Caffey's syndrome, Caffey-Silverman syndrome.
(05 Mar 2000)
Caffey's syndrome Neonatal subperiosteal bone formation over many bones, especially the mandible and clavicles and the shafts of long bones; it follows fever, usually appearing before 6 months of age and disappearing during childhood.
Synonym: Caffey's disease, Caffey's syndrome, Caffey-Silverman syndrome.
(05 Mar 2000)
camptomelic syndrome <syndrome> Also associated with flat facies, short vertebrae, hypoplastic scapula, and bowed tibia.
Synonym: osteochondrodysplasia.
(05 Mar 2000)
cantrell syndrome <radiology> Herniation of gut into pericardial sac, common anterior communication in diaphragm and pericardium, associated with congenital defects of sternum, heart, mesentery, anterior abdominal wall, must be excluded in presence of omphalocele, ** diaphragmatic hernia
(12 Dec 1998)
capgras syndrome <syndrome> A psychotic disorder characterised by the patient's conviction that certain important or familiar persons in his environment are not real but are "doubles" of themselves or imposters.
(12 Dec 1998)
Capgras' syndrome <syndrome> The delusional belief that a person (or persons) close to the schizophrenic patient has been substituted for by one or more impostors; may have an organic aetiology.
Synonym: Capgras' phenomenon, illusion of doubles.
(05 Mar 2000)
capillary leak syndrome <syndrome> Extravasation of plasma fluid and proteins into the extravascular space, resulting in sometimes fatal hypotension and reduced oxygen perfusion. Clinical capillary leak syndrome is observed in patients who demonstrate a state of generalised leaky capillaries following shock syndromes, low-flow states, ischemia-reperfusion injuries, toxaemias, or poisoning. It can lead to generalised oedema and multiple organ failure., reperfusion injuries and clinical capillary leak syndrome.
(12 Dec 1998)
caplan's syndrome <syndrome> Pneumoconiosis associated with rheumatoid arthritis.
(12 Dec 1998)
caplan syndrome <radiology> Combination of: necrobiotic rheumatoid lung nodules, coal worker's pneumoconiosis Findings: round, peripheral nodules (0.5 - 5.0 cm), with or without cavitation, nodules associated with subcutaneous rheumatoid nodules
(12 Dec 1998)
carbohydrate-deficient glycoprotein syndrome <syndrome> An inborn error of carbohydrate metabolism manifesting as a genetic multisystem disorder of autosomal recessive inheritance. A predominant feature is severe central and peripheral nervous system involvement resulting in psychomotor retardation, seizures, cerebellar ataxia, and other symptoms which include growth retardation, retinitis pigmentosa, hypothyroidism, and fatty liver. The notable biochemical feature is the deficiency of a large number of blood glycoproteins and decreased activities of various blood coagulation factors.
(12 Dec 1998)
carbonic anhydrase II deficiency syndrome <syndrome> An inherited deficiency of carbonic anhydrase II that results in osteopetrosis and metabolic acidosis.
Synonym: osteopetrosis with renal tubular acidosis.
(05 Mar 2000)
carcinoid syndrome <oncology, syndrome> A constellation of symptoms associated with a serotonin-secreting neoplasm known as carcinoid tumour.
These tumours may grow anywhere in the gastrointestinal tract (and in the lungs) with approximately 90% in the appendix. The remainder occur in the ileum, stomach, colon or rectum.
Symptoms include flushing, rapid pulse, facial swelling, swelling around the eyes, low blood pressure, abdominal pain, weight loss and diarrhoea.
(19 Jan 1998)
cardiofacial syndrome <syndrome> Transient or persistent unilateral partial lower facial paresis accompanying some congenital heart disease.
A group of syndromes characterised by congenital cardiovascular, bone, soft tissue, and facial abnormalities. Examples include Rubinstein-Taybi syndrome, Noonan's syndrome and Williams' syndrome.
Synonym: Williams' syndrome.
(05 Mar 2000)
carney syndrome <radiology> Association of: pheochromocytoma, paraganglioma (functioning), chondroma (mult. Chondromatous hamartomas?)
(12 Dec 1998)
Caroli's syndrome <syndrome> Congenital malformation of the bile ducts leading to formation of multifocal dilatations and cysts.
(05 Mar 2000)
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