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"prodrmal radiation 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
  • Horner¡¯s syndrome
    È£³ÊÁõÈıº
  • Hunter¡¯s syndrome
    ÇåÅÍÁõÈıº
  • Hurler¡¯s syndrome
    Çæ·¯ÁõÈıº
  • iridocorneal endothelial syndrome
    ȫä°¢¸·³»ÇÇÁõÈıº
  • irritable bowel syndrome
    °ú¹Î´ëÀåÁõÈıº
  • immotile cilia syndrome
    ºÎµ¿¼¶¸ðÁõÈıº
  • impingement syndrome
    ºÎµúÈûÁõÈıº, Ãæµ¹ÁõÈıº
  • idiopathic respiratory distress syndrome
    Ư¹ßÈ£Èí°ï¶õÁõÈıº
  • intracerebral steal syndrome
    ³ú³»Ç÷·ù»©¾Ñ±èÁõÈıº
  • Jadassohn-Lewandowsky syndrome
    ¾ß´Ù½ºÁ¸-·¹¹Ýµµºê½ºÅ°ÁõÈıº
  • jet lag syndrome
    ½ÃÂ÷ÁõÈıº
  • Kallmann syndrome
    Ä®¸¸ÁõÈıº
  • Kartagener¡¯s syndrome
    Ä«¸£Å¸°Ô³ÊÁõÈıº
  • Klinefelter¡¯s syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº
  • Klippel-Feil syndrome
    Ŭ¸®Æç-ÆÄÀÏÁõÈıº
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    ÇѱÛ
  • fertile eunuch syndrome
    °¡ÀÓ°íÀÚÁõÈıº
  • fetal alcohol syndrome
    žƾËÄÚ¿ÃÁõÈıº
  • fetal distress syndrome
    žưíÅëÁõÈıº, žÆÀý¹Ú°¡»çÁõÈıº
  • fish-eye syndrome
    ¹°°í±â´«ÁõÈıº
  • 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
  • general adaptation syndrome
    Àü½Å¼øÀÀÁõÈıº
  • 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
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 14
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  • DaCostas syndrome
    ´ÙÄÚ½ºÅ¸ ÁõÈıº(~ñøý¦ÏØ)
  • De Sanctis-Caccione syndrome = xerodermic idiocy
    °ÇÇǼº ¹éÄ¡
  • Defibrillation syndrome
    Å»¼¶À¯¼ÒÁõÈıº
  • Devies syndrome
    µ¥ºòÁõÈıº
  • Di Guglielmo syndrome
    µð±¸±Û¸®¿¤¸ðÁõÈıº, ÀûÇ÷º´¼º °ñ¼öÁõ
  • DiGeorges syndrome => thymic-parathyroid aplasia
    µðÁÒÁö ÁõÈıº
  • Dorfman-Chanarin syndrome = neutral lipid storage disease
    Áß¼ºÁö¹æÃàÀûÁõ
  • Down syndrome
    ´Ù¿îÁõÈıº
  • Downs syndrome
    ´Ù¿îÁõÈıº
  • Downs syndrome
    ´Ù¿î ÁõÈıº
  • Duanes retraction syndrome
    µà¾È¾È±¸ÈÄÅðÁõÈıº
  • Dubin-Johnson syndrome
    µàºó-Á¸½¼ÁõÈıº.
  • Edwards syndrome
    ¿¡µå¿öÁîÁõÈıº.
  • Ehlers-Danlos syndrome
    ¿¤·¯½º-´Ü·Î½º ÁõÈıº
  • Fanconi syndrome
    ÆÇÄÚ´Ï ÁõÈıº(ñøý¦ÏØ)
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  • supervoltage radiation
    ÃʰíÀü¾Ð
  • target skin distance radiation
    Ç¥ÀûÇǺΰŸ®¹æ»ç¼±
  • temperature radiation
    ¿Âµµº¹»ç(è®öôÜßÞÒ).
  • terrestrial radiation
    Áö±¸¹æ»ç¼±
  • thermal radiation
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  • ultraviolet radiation
    Àڿܼ±º¹»ç(¡­ÜßÞÒ).
  • ultraviolet radiation
    Àڿܼ±º¹»ç(¡­ÜßÞÒ)
  • ultraviolet radiation
    Àڿܼ±(í¹èâàÊ)Á¶»ç
  • whole liver radiation
    Àü°£Á¶»ç
  • abdominal muscle deficiency syndrome
    º¹±Ù°á¼ÕÁõÈıº(ÜÙÐÉÌÀáßñøý¦ÏØ).
  • absent pulmonary valve syndrome
    Æóµ¿¸ÆÆÇ°á¿©Áõ.
  • absent pulmonary valve syndrome
    Æóµ¿¸ÆÆÇ°á¿©Áõ.
  • absent testes syndrome
    °íȯ°á¿©ÁõÈıº
  • abstinence syndrome
    ±Ý´ÜÁõÈıº(Ð×Ó¨ñøý¦ÏØ).
  • acid aspiration syndrome
    À§»ê ÈíÀÔ ÁõÈıº
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NCRP National Council on Radiation Protection [and Measurements]
NCRV National Committee for Radiation Victims
NERO noninvasive evaluation of radiation output
NR do not repeat [Lat. non repetatur]; nerve root; neural retina; neutral red; noise reduction; nonreac...
OR a logical binary relation that is true if any argument is true, and false otherwise; [o]estrogen rec...
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BBS BARDET-Biedl syndrome
BLS Bare Lymphocyte Syndrome
BS Bartter syndrome
BCNS Basal Cell Nevus Syndrome
BWS Beckwith Wiedemann Syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 14
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  • 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
  • Digeorge syndrome
    Digeorge ÁõÈıº
    À¯Àü¼º ¸é¿ª °á¼ÕÀÇ ÇÑ Á¾·ù·Î Èä¼± Çü¼º ºÎÀü°ú ¼¼Æ÷¼º ¸é¿ª ±â´ÉÀÇ °¨¼Ò·Î ³ªÅ¸³­´Ù.
  • discrete multiple endocrine adenomatosis syndrome
    ºÐ¸®¼º ´Ù¹ß ³»ºÐºñ ¼±Á¾ ÁõÈıº
  • dorsal midbrain syndrome
    ÈÄÁß³ú ÁõÈıº
  • double crush syndrome
    ÀÌÁß ºÐ¼â ÁõÈıº
  • Dresslers syndrome
    µå·¹½½·¯ ÁõÈıº
  • Duanes retraction syndrome
    µà¾È ¾È±¸ ÈÄÅð ÁõÈıº
  • dysconnection syndrome
    ºÐ¸® ÁõÈıº
  • dyskinetic syndrome
    ¿îµ¿ Àå¾Ö ÁõÈıº
  • dysplastic nevus syndrome
    ÀÌÇü¼º ¸ð¹Ý ÁõÈıº
  • dysuria-pyuria syndrome
    ¹è´¢ Àå¾Ö-³ó´¢ ÁõÈıº
  • early postprandial postgastrectomy syndrome
    Á¶±â ½ÄÈļº À§ ÀýÁ¦ ÈÄ ÁõÈıº
  • eaton-lambert syndrome
    ÀÌÆ°-¶÷¹öÆ® ÁõÈıº
  • ectopic ACTH syndrome
    À̼Ҽº ºÎ½Å ÇÇÁú ÀÚ±Ø È£¸£¸ó ÁõÈıº, À̼Ҽº ACTH ÁõÈıº
    ACTHÀÇ °úÀ× »ý»ê, Á߽ɼº ºñ¸¸, ¸¸¿ùÇü ¾ó±¼, °íÇ÷¾Ð µîÀÇ Áõ»óÀÌ ³ªÅ¸³­´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 14
Beuren syndrome <syndrome> Supravalvular aortic stenosis with multiple areas of peripheral pulmonary arterial stenosis, mental retardation, and dental anomalies.
(05 Mar 2000)
Biemond syndrome <syndrome> Iris coloboma, mental retardation, obesity, hypogenitalism, and postaxial polydactyly; a recessive inheritance disorder resembling Laurence-Moon and Bardet-Biedel syndrome's.
(05 Mar 2000)
billowing mitral valve syndrome <syndrome> The clinical constellation of findings with or without symptoms due to prolapse of the mitral valve: a nonejection systolic click accentuated in the standing posture, sometimes multiple, sometimes with mitral regurgitation occurring relatively late in systole, and accompanied by echocardiographic evidence of the mitral valve prolapse, usually with thickened leaflets of the valve. Symptoms are non-specific and may include vague chest pains and dyspnea on exertion.
Synonym: billowing mitral valve syndrome.
(05 Mar 2000)
Bjornstad's syndrome <syndrome> Pili torti associated with sensorineural hearing loss, the severity of distortion and brittleness of the hair correlated with the degree of deafness; autosomal dominant inheritance.
(05 Mar 2000)
Blatin's syndrome The peculiar trembling or vibratory sensation felt on palpation of a hydatid cyst.
Synonym: Blatin's syndrome, hydatid fremitus.
(05 Mar 2000)
blind loop syndrome <syndrome> Malabsorption, especially of vitamin b12 or folic acid, due to metabolic competition by bacteria proliferating in a segment of small intestine excluded from normal peristaltic movement; it may occur as a postoperative complication of side-to-side anastomosis of intestine, as a result of intestinal diverticula, fistula, etc.
(12 Dec 1998)
Bloch-Sulzberger syndrome A genetic disease with blisters that develop soon after birth on the trunk and limbs, then heal, but leave dark (hyperpigmented) streaks and marble-like whorls on the skin. (the name came from the erroneous idea that the skin cells were incontinent of pigment and could not contain it normally.) other key features of ip include dental and nail abnormalities, bald patches, and (in about 1/3rd of cases) mental retardation. Ip is an x-linked dominant with male lethality. The ip gene is in band q28 on the x chromosome. Mothers with ip have an equal chance of having a normal or ip daughter or a normal son. The ip sons die before birth. Ip is also known as bloch-sulzberger syndrome.
(12 Dec 1998)
Bloom's syndrome <syndrome> Congenital telangiectatic erythema, primarily in butterfly distribution, of the face and occasionally of the hands and forearms, with sensitivity of skin lesions and dwarfism with normal body proportions except for a narrow face and dolichocephalic skull; chromosomes are excessively fragile; autosomal recessive inheritance.
(05 Mar 2000)
bloom syndrome <syndrome> An autosomal recessive disorder characterised by telangiectatic erythema of the face, photosensitivity, dwarfism, and other abnormalities.
(12 Dec 1998)
blue rubber bleb nevus syndrome <radiology> Bean syndrome, sporadic (some autosomal dominant), rubbery, raised blue-black skin nevi (cavernous haemangiomata, 0.1 - 5 cm), GI mucosal haemangiomata, bowel: polypoid filling defects of varying sizes, visceral haemangiomata (by angio) associated with: leukaemia, medulloblastoma, hypernephroma, Mafucci syndrome More info: blue rubber bleb nevus syndrome
(12 Dec 1998)
blue toe syndrome <syndrome> Atherothrombotic microembolism of the lower extremities due to recurrent cholesterol embolic 'showers' with painful cyanotic discoloration of the toes and embolism to other sites that completely resolve between attacks. Despite the gangrene-like appearance, blue toes may respond to conservative therapy without amputation.
(12 Dec 1998)
Boerhaave's syndrome <syndrome> Named after Captain Boerhaave, a Dutch ship captain, who was the first patient this condition was described in. Traumatic rupture of the lower oesophagus can occur with significant blunt chest trauma, during CPR or in some conditions of forceful protracted vomiting. This condition is much more common in the patient with a pre-existing oesophageal disease such as reflux oesophagitis. The chest X-ray will typically show an abnormal left cardiac border with free fluid within the left hemithorax (pleural effusion). Patients will experience immediate chest pain, which may radiate to the neck, accompanied by shock, sepsis and death within 48 hours if untreated.
(27 Sep 1997)
boerhaave syndrome <radiology> Complete, transmural laceration of oesophagus, aetiology: spontaneous (retching, EtOH), secondary to endoscopy, trauma, vagotomy, FB, symptoms: chest pain, shock, dyspnea, cyanosis, grave prognosis, M more than F, usually on left, uncommonly sub-diaphragmatic see also: oesophageal trauma, V sign of Naclerio
(12 Dec 1998)
Bonnevie-Ullrich syndrome <syndrome> A rare genetic disorder in women that is characterised by the absence of an X chromosome.
This disorder inhibits normal sexual development and causes infertility. Features include webbing of the neck, short stature, retarded development of secondary sex characteristics, absence of menses, coarctation of the aorta, low hairline, eye abnormalities (drooping eyelids) and skeletal deformities.
Treatment include oestrogen supplementation at puberty. Growth hormone replacement may be necessary in some cases. Cardiac surgery may be necessary to correct coarctation of the aorta.
Incidence: 1 in 3000 births.
(27 Sep 1997)
Bonnier's syndrome <syndrome> A syndrome due to a lesion of Deiters nucleus and its connection; the symptoms include ocular disturbances (e.g., paralysis of accommodation, nystagmus, diplopia), as well as deafness, nausea, thirst, anorexia, and symptoms referable to the involvement of the vagus centres.
(05 Mar 2000)
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