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"ectrodactyly-ectodermal dysplasia clefting 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.
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
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  • ¿µ¹®
    ÇѱÛ
  • 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
  • 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
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 9 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
  • 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
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
  • 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.
  • XXYY syndrome
    XXYYÁõÈıº.
  • Zieves syndrome
    ÁöºêÁõÈıº
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
  • co-contraction syndrome
    µ¿½Ã¼öÃàÁõÈıº
  • 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).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
FGDY faciogenital dysplasia
FND febrile neutrophilic dermatosis; frontonasal dysplasia
GHDD ghosal hematodiaphyseal dysplasia
GUD genitourinary dysplasia
HEPOD hereditary expansile polyostotic dysplasia
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
CFS Chronic Fatigue Syndrome
CPPS Chronic Pelvic Pain Syndrome
CSS Churg Strauss Syndrome
CS Cocayne syndrome
CLS Coffin-Lowry syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
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    ¼³¸í
  • lacunar syndrome
    ¼Ò°ø¼º °æ»ö ÁõÈıº
  • Lafora syndrome
    ¶óÆ÷¶ó ÁõÈıº
  • Lambert-Eaton myasthenic syndrome
    ¶÷¹öÆ®-ÀÌÆ° ±Ù¹«·ÂÁõ ÁõÈıº
  • landry-guillain-barre syndrome
    ¶õµå¸®-±æ·©-¹Ù·¹ ÁõÈıº
  • laryngo-onycho-cutaneous syndrome
    ÈĵÎ-¼Õ ¹ßÅé-ÇǺΠÁõÈıº
  • lateral cord and associated anterior cornual syndrome
    Ãø»è µ¿Ãø Àü°¢ ÁõÈıº
  • lateral medullary syndrome
    ¿¬¼ö ¿ÜÃø ÁõÈıº, ¿ÜÃø ¿¬¼ö ÁõÈıº
    ¿¬¼öÀÇ ¿ÜÃøºÎ°¡ Ç÷°ü Àå¾Ö, µå¹°°Ô Á¾¾ç, ¿°Áõ, Å»¼ö µî¿¡ ÀÇÇØ ±âÁúÀû º¯È­¸¦ ÀÏÀ¸Å°°í ƯÀ¯ÇÑ Áõ»óÀ» ³ªÅ¸³»´Â °æ¿ì.
  • lazy bladder syndrome
    Ÿ¸ ¹æ±¤ ÁõÈıº
  • lazy leukocyte syndrome
    Ÿ¸ ¹éÇ÷±¸ ÁõÈıº
    È£Áß±¸ ±â´É ÀÌ»ó°ú À¯»çÇÑ ÀÓ»ó Áõ»óÀ» º¸ÀÌ´Â ¹éÇ÷±¸ »óÀÇ Áúº´.
  • Leigh syndrome
    ·¹ÀÌ ÁõÈıº
  • Leriche's syndrome
    Leriche¾¾ ÁõÈıº
    ´ç´¢ ȯÀÚ¿¡¼­ÀÇ ¹ß±â ºÎÀüÀº ºÎÀûÀýÇÑ À½°æ Ç÷·ù³ª ÀÚÀ²½Å°æ º´Áõ°ú °ü°è°¡ ÀÖ´Ù. Ç÷°ü ÁúȯÀº ³ëÀο¡¼­ ³ªÅ¸³ª´Â ¹ß±â ºÎÀüÀÇ ÈçÇÑ ¿äÀÎÀÌ´Ù. ¹ß±â ºÎÀü°ú ÇÔ²² ÇÏÁö¿¡ Ç÷¾× ¼øÈ¯ Àå¾Ö¿¡ ÀÇÇÑ ÆÄÇàÀÌ µ¿¹ÝµÈ °æ¿ì°¡ À̺´¿¡ ÇØ´çÇÑ´Ù.
  • Lesch-Nyhan syndrome
    ·¹½¬ ´ÏÇÑ ÁõÈıº
    ¹Ý¼º À¯Àü ÁúȯÁßÀÇ Çϳª·Î È¿¼Ò°¡ °áÇÌµÇ¾î Æ¯Á¤ ¹°ÁúÀÌ Á¤»óº¸´Ù ¸¹ÀÌ »ý»êµÇ¾î ¹ßº´ÇÑ´Ù. hy
  • Leser-Trelat syndrome
    ·¹Á¦¸£ Æ®·¼¶ó ÁõÈıº
  • Letterer-Siwe syndrome
    ·¹Å×·¯-½Ã¿þ ÁõÈıº
  • Libman Sachs syndrome
    ¸®ºê¸¸-ÀÛ½º ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
Mad Hatter syndrome <syndrome> Gastrointestinal and central nervous system manifestations of chronic mercury poisoning, including stomatitis, diarrhoea, ataxia, tremor, hyperreflexia, sensorineural impairment, and emotional instability; previously seen in workers in lead manufacturing who put mercury-containing materials in their mouths to make them more pliable.
Origin: fr. Char. In Alice in Wonderland
(05 Mar 2000)
Maffucci's syndrome <syndrome> Enchondromatosis with multiple cavernous haemangiomas.
Synonym: dyschondroplasia with haemangiomas.
(05 Mar 2000)
Mafucci syndrome <syndrome> Rare, multiple enchondromata, 40 - 45% malignant transformation leading to chondrosarcoma, multiple cavernous haemangiomata, may degenerate leading to angiosarcoma Cf: Ollier disease
(12 Dec 1998)
Magendie-Hertwig syndrome <clinical sign> Skew deviation of the eyes in acute cerebellar lesions.
Synonym: Magendie-Hertwig syndrome.
(05 Mar 2000)
van Buchem's syndrome <syndrome> An inherited skeletal dysplasia, with mandibular enlargement and thickening of the diaphyses and calvaria, and increased serum alkaline phosphatase; autosomal recessive inheritance.
Synonym: generalised cortical hyperostosis.
(05 Mar 2000)
paleostriatal 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)
van der Hoeve's syndrome <syndrome> A subtype of osteogenesis imperfecta in which progressive conductive hearing loss begins in childhood because of stapedial fixation.
(05 Mar 2000)
vanished testis syndrome <syndrome> Absence of both testes in a male with normal chromosomes (XY) and otherwise normal genitalia at birth and during childhood. Testes were present in at least the first trimester of gestation, but vanished sometime thereafter.
(05 Mar 2000)
vanishing lung syndrome <syndrome> Progressive decrease of radiographic opacity of the lung caused by accelerated development of emphysema or rapid cystic destruction of the lung from infection.
(05 Mar 2000)
pallidal 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)
pallister-killian syndrome <syndrome> A condition with multiple malformations at birth and mental retardation due to isochromosome 12p mosaicism (an abnormal chromosome 12 in some cells).
(12 Dec 1998)
Raeder's paratrigeminal syndrome <syndrome> A postganglionic Horner's syndrome associated with trigeminal nerve dysfunction caused by involvement of the carotid sympathetic plexus, near Mechel' cave.
(05 Mar 2000)
Ganser's syndrome <syndrome> A psychotic-like condition, without the symptoms and signs of a traditional psychosis, occurring typically in prisoners who feign insanity; e.g., such a person, when asked to multiply 6 by 4, will give 23 as the answer, or he will call a key a lock.
See: malingering, factitious disorder.
Synonym: nonsense syndrome, syndrome of approximate relevant answers, syndrome of deviously relevant answers.
(05 Mar 2000)
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)
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