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"functional prepubertal castration 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
  • Klinefelter¡¯s syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº
  • Klippel-Feil syndrome
    Ŭ¸®Æç-ÆÄÀÏÁõÈıº
  • Korsakoff¡¯s syndrome
    ÄÚ¸£»çÄÚÇÁÁõÈıº
  • Kearns-Sayre syndrome
    ÄÁ½º-¼¼À̾îÁõÈıº
  • late dumping syndrome
    ¸¸±â´ýÇÎÁõÈıº
  • Laurence-Moon syndrome
    ·Î·»½º-¹®ÁõÈıº
  • Lennox-Gastaut syndrome
    ·¹³ì½º-°¡½ºÅäÁõÈıº
  • Lesch-Nyhan syndrome
    ·¹½´-´ÏÇÑÁõÈıº
  • Libman-Sacks syndrome
    ¸®ºê¸Õ-»è½ºÁõÈıº
  • locked-in syndrome
    °¨±ÝÁõÈıº
  • long QT syndrome
    ±äQTÁõÈıº
  • lymphadenopathy syndrome
    ¸²ÇÁÀýº´(Áõ)ÁõÈıº
  • lymphoproliferative syndrome
    ¸²ÇÁ¼¼Æ÷Áõ½ÄÁõÈıº
  • middle lobe syndrome
    Áß°£¿±ÁõÈıº
  • milk-alkali syndrome
    ¿ìÀ¯¾ËÄ®¸®ÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 13
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    ÇѱÛ
  • myelodysplastic syndrome
    °ñ¼öÇü¼ºÀÌ»óÁõÈıº
  • myeloproliferative syndrome
    °ñ¼öÁõ½ÄÁõÈıº
  • myofascial click pain syndrome
    ±Ù¸·ÅëÁõÁõÈıº
  • myotonic syndrome
    ±ÙÀ°±äÀåÁõÈıº
  • naviculocapitate syndrome
    ¼Õ¹è¾Ë¸Ó¸®»ÀÁõÈıº
  • nephrotic syndrome
    ÄáÆÏÁõÈıº
  • neuroleptic malignant syndrome
    Ç×Á¤½Åº´¾à¹°¾Ç¼ºÁõÈıº
  • neurovascular syndrome
    ½Å°æÇ÷°üÁõÈıº
  • neurovisceral syndrome
    ½Å°æ³»ÀåÁõÈıº
  • nutritional deficiency syndrome
    ¿µ¾ç°áÇÌÁõÈıº
  • obstructive sleep apnea syndrome
    Æó¼â¼ö¸é¹«È£ÈíÁõÈıº
  • oculoauriculovertebral syndrome
    ´«±Ó¹ÙÄûôÃßÁõÈıº
  • oral-facial-digital syndrome
    ÀÔ¾ó±¼¼Õ°¡¶ôÁõÈıº, ±¸°­¾È¸é¼öÁ·ÁöÁõÈıº
  • orbital apex syndrome
    ´«È®²ÀÁöÁõÈıº
  • organic brain syndrome
    ±âÁú³úÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 13
  • ¿µ¹®
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  • Hutchinson Gilford syndrome
    ÇãÄ£½¼-±æÆ÷¿ÀµåÁõÈıº.
  • Hutchinson-Gilford syndrome => progeria
    ÇãÄ£½¼-±æÆ÷µå ÁõÈıº
  • Imerslund-Gra sbeck syndrome
    À̸ӽ½·éµå-±×·¹½ºº£Å© ÁõÈıº
  • Irvine-Gass syndrome
    ¾î¹ÙÀÎ-°¡½º ÁõÈıº
  • Job-Buckley syndrome
    Á¼-¹öŬ¸® ÁõÈıº
  • Kallmann syndrome
    Ä®¸¸ÁõÈıº
  • Kanners syndrome
    Ä­³ÊÁõÈıº(~ñøý¦ÏØ)
  • Kassabach-Meritt syndrome
    Ä«»ç¹ÙÇÏ-¸Þ¸®Æ® ÁõÈıº
  • Kawasaki disease => mucocutaneous lymph node syndrome
    °¡¿Í»çŰ º´
  • Kernohan s syndrome
    Ä¿³ëÇÑÁõÈıº.
  • Kinky hair syndrome
    ŲŰÇì¾îÁõÈıº
  • Klinefelter s syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº.
  • Klinefelters syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº
  • Klinefelters syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº(¡­ñøý¦ÏØ)
  • Klippel Feli syndrome
    Ŭ¸®Æç-ÆäÀÏÁõÈıº.
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 13
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  • bradycardia tachycardia syndrome
    ¼øÈ¯¼­¸Æºó¸ÆÁõÈıº.
  • bradytachycardia syndrome
    ¼­ºó¸ÆÁõÈıº(ßïÞºØæñøý¦ÏØ).
  • brain death syndrome
    ³ú»çÁõÈıº(ÒàÞÝñøý¦ÏØ).
  • 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) .
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 13
FRV full-length retroviral [sequence]; functional residual volume
FSI foam stability index; Food Sanitation Institute; functional status index; function status index
FSN functional stimulation, neuromuscular
FSQ Functional Status Questionnaire
FSRS functional status rating system
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 13
BCNS Basal Cell Nevus Syndrome
BWS Beckwith Wiedemann Syndrome
BS Behcet's Syndrome
BSS Bernard Soulier Syndrome
BPES Blepharophimosis Ptosis Epicanthus inversus Syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 13
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    ¼³¸í
  • 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.
  • ectopic Cushing's syndrome
    À̼Ҽº Äí½Ì ÁõÈıº
  • Edinger-Westphal syndrome
    ¿¡µù°Å-¿þ½ºÆ®ÆÈ ÁõÈıº
  • effort syndrome
    ¿¡Æ÷Æ® ÁõÈıº
  • electrolyte deficiency syndrome
    ÀüÇØÁú °áÇÌ ÁõÈıº
  • empty sella syndrome
    °ø Å;îŰ¾È ÁõÈıº
    °¡Àå ÈçÇϰԴ ÁöÁÖ¸·ÀÌ Å;îŰ¾È Ⱦ°Ý¸·ÀÇ °á¼ÕºÎ¸¦ ÅëÇÏ¿© ºüÁ® µé¾î¿À´Â °ÍÀε¥ Çϼöü °æÀÌ Áö³ª´Â ±¸¸ÛÀÌ Å©´ÙµçÁö ¶Ç´Â ´Ù¸¥ °á¼ÕºÎ°¡ ÀÖ¾î ÀϾ´Ù. ³ú ô¼ö¾×¾ÐÀ¸·Î ÀÎÇØ Çϼöü°¡ À§ÃàµÇ°í Å;îŰ¾ÈÀº ºó ¸ð½ÀÀÌ µÈ´Ù. ´Ù¸¥ ¿øÀÎÀ¸·Î´Â Sheehan ÁõÈıº, ¼±Á¾ÀÇ ¿ÏÀü °æ»ö ÈÄ ¼¶À¯¼º ¹ÝÈçÈ­ ±×¸®°í ¼ö¼úÀ̳ª ¹æ»ç¼±Àû Çϼöü ÀýÁ¦ µîÀÌ´Ù. ´ë°³ ȯÀÚ´Â Çϼöü ºÎÀüÀ» ¹æÁöÇÒ ¸¸ÇÑ ÃæºÐÇÑ ½ÇÁúÀÌ º¸Á¸µÈ´Ù. ±×·¯³ª ¶§·Î´Â Ç⼺ È£¸£¸ó ÇÑ Á¾·ù ¶Ç´Â ±× ÀÌ»óÀÇ ºÐºñ ºÎÁ·ÀÌ ÀÖ´Ù.
  • encephalitis syndrome
    ³ú¿° ÁõÈıº
  • encephalotrigeminal syndrome
    ³ú »ïÂ÷ ½Å°æ ÁõÈıº
  • eosinophilia myalgia syndrome
    È£»ê±¸¼º ±ÙÀ°Åë ÁõÈıº, È£»ê±¸ Áõ´Ù¼º ±ÙÀ°Åë ÁõÈıº
  • eosinophilic pulmonary syndrome
    È£»ê¼º Æó ÁõÈıº
    ¸¸¼º È£»ê±¸¼º Æó·ÅÀº ÆóÆ÷ ¼¼Ã´À̳ª »ý°Ë»ó È£»ê±¸°¡ Æó Á¶Á÷ÀÇ ¸»Ãʺο¡ Ä§ÂøµÈ ¼Ò°ßÀ» Ư¡À¸·Î ÇÏ´Â ÁõÈıºÀ» ÀǹÌÇÑ´Ù. Ç÷¾× È£»ê±¸ Áõ°¡°¡ ´ëºÎºÐ °üÂûµÈ´Ù. ¸¸¼º È£»ê±¸¼º Æó·ÅÀº ÁÖ·Î ¿©ÀÚ¿¡ ³ªÅ¸³ª¸ç, ¹ß¿­, ¹ßÇÑ, üÁß °¨¼Ò, È£Èí °ï¶õÀÌ Æ¯Â¡ÀÌ´Ù. Ä¡·á´Â °æ±¸
  • epidermal nevus syndrome
    Ç¥ÇÇ ¸ð¹Ý ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 13
Briquet's syndrome <syndrome> A chronic but fluctuating mental disorder, usually of young women, characterised by frequent complaints of physical illness involving multiple organ systems simultaneously.
(05 Mar 2000)
Brissaud-Marie syndrome <syndrome> Unilateral spasm of the tongue and lips, of hysterical nature.
(05 Mar 2000)
Brock's syndrome Atelectasis of the right middle pulmonary lobe, with chronic pneumonitis.
(12 Dec 1998)
Brown-Sequard's syndrome <neurology, syndrome> A type of spinal cord lesion that is characterised by hemiparaplegia and hyperesthesia, but with loss of motor function on the same side as the lesion and hemianaesthesia on the opposite side.
(27 Sep 1997)
brown-sequard syndrome <syndrome> A syndrome due to damage of one half of the spinal cord, resulting in ipsilateral paralysis below the level of the lesion and loss of discriminatory and joint sensation, and contralateral loss of pain and temperature sensation. Brown-sequard was a french physiologist, 1817-1894. The syndrome is also called brown-sequard disease and brown-sequard paralysis but this latter should not be confused with a flaccid paralysis seen in disorders of the urinary tract called by the same name.
(12 Dec 1998)
brown's syndrome <syndrome> An ophthalmology (eye) problem. Brown's syndrome presents as an abnormality at birth (congenitally) and is characterised by an inability to elevate the eyeball when also trying to move the eyeball to the outside. Brown's syndrome can also occur because of other conditions which affect the normal function of the eye muscles.
(12 Dec 1998)
Brugsch's syndrome <radiology> Idiopathic, familial hypertrophic osteoarthropathy, boys at puberty, blacks more than whites, familial, periosteal reaction, thick skin: extremities and forehead, hyperhidrosis, relatively pain free
(12 Dec 1998)
Budd-Chiari syndrome <gastroenterology, syndrome> Liver dysfunction due to occlusion of the hepatic veins. May be congenital.
(27 Sep 1997)
Budd's syndrome <syndrome> Thrombosis of the hepatic vein with great enlargement of the liver and extensive development of collateral vessels, intractable ascites, and severe portal hypertension.
Synonym: Budd's syndrome, Budd-Chiari syndrome, Chiari's disease, Chiari-Budd syndrome, Rokitansky's disease.
(05 Mar 2000)
Burger-Grutz syndrome Hyperlipoproteinaemia characterised by the presence of large amounts of chylomicrons and triglycerides in the plasma when the patient has a normal diet, and their disappearance on a fat-free diet; low alpha-and beta-lipoproteins on a normal diet, with increase on fat-free diet; decreased plasma postheparin lipolytic activity; and low tissue lipoprotein lipase activity. It is accompanied by bouts of abdominal pain, hepatosplenomegaly, pancreatitis, and eruptive xanthomas; autosomal recessive inheritance.
See: familial lipoprotein lipase inhibitor.
Synonym: Burger-Grutz syndrome, familial fat-induced hyperlipaemia, familial hyperchylomicronaemia, familial hypertriglyceridemia, idiopathic hyperlipaemia.
(05 Mar 2000)
burner syndrome <syndrome> Multiple episodes of upper extremity burning pain, sometimes accompanied by shoulder girdle weakness, experienced during contact sports, especially football, with each forceful blow to the head or shoulder; attributed to an upper trunk brachial plexopathy.
(05 Mar 2000)
Burnett's syndrome <syndrome> A form of metabolic acidosis that can result from the excessive consumption of milk (calcium) and antacids (sodium bicarbonate) over a prolonged period of time. This can result in calcium deposits in the kidneys and body tissues.
Symptoms include nausea, vomiting and weakness. May be seen as a complication of peptic ulcer therapy.
(27 Sep 1997)
burning foot syndrome <syndrome> A disorder observed in prisoners-of-war in World War II, now believed to be due to a pantothenate deficiency.
(05 Mar 2000)
burning mouth syndrome <syndrome> A group of painful oral symptoms associated with a burning or similar sensation. There is usually a significant organic component with a degree of functional overlay; it is not limited to the psychophysiologic group of disorders.
(12 Dec 1998)
burning vulva syndrome <syndrome> Persistent vulvodynia in which a physical cause has not been identified.
(05 Mar 2000)
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