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  • ¿µ¹®
    ÇѱÛ
  • nutritional deficiency syndrome
    ¿µ¾ç°áÇÌÁõÈıº
  • Ogilvie syndrome
    ¿À±æºñÁõÈıº
  • oral-facial-digital syndrome
    ÀÔ¾ó±¼¼Õ°¡¶ôÁõÈıº, ±¸°­¾È¸é¼öÁ·ÁöÁõÈıº
  • orbital apex syndrome
    ´«È®²ÀÁöÁõÈıº, ¾È¿Í÷´ÜÁõÈıº
  • organic mental syndrome
    ±âÁú¼ºÁ¤½ÅÁõÈıº
  • Osler-Weber-Rendu syndrome
    ¿À½½·¯-¿þ¹ö-¶ûµÚÁõÈıº
  • obstructive sleep apnea syndrome
    Æó¼â¼ö¸é¹«È£ÈíÁõÈıº
  • overlap syndrome
    °ãħÁõÈıº, Áߺ¹ÁõÈıº
  • overuse syndrome
    °ú»ç¿ëÁõÈıº, °ú¿ëÁõÈıº
  • overwear syndrome
    °úµµÂø¿ëÁõÈıº
  • Pancoast syndrome
    ÆÒÄÚ½ºÆ®ÁõÈıº
  • Pickwickian syndrome
    ÇÈÀ¨ÁõÈıº
  • Pierre Robin syndrome
    ÇÇ¿¡¸£·Î¹ðÁõÈıº
  • placental transfusion syndrome
    ŹݼöÇ÷ÁõÈıº
  • polycystic ovarian syndrome
    ´Ù³¶³­¼ÒÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • punch-drunken syndrome
    (¢¡boxer¡¯s dementia) ±ÇÅõ¼±¼öÄ¡¸Å
  • quadrilateral space syndrome
    ³×¸ð°ø°£ÁõÈıº
  • radicular syndrome
    ½Å°æ»Ñ¸®ÁõÈıº
  • respiratory distress syndrome
    È£Èí°ï¶õÁõÈıº
  • retraction syndrome
    ¾È±¸ÈÄÅðÁõÈıº
  • rotator cuff syndrome
    ȸÀü±Ù°³ÁõÈıº, ±ÙÀ°µÑ·¹¶ìÁõÈıº
  • rubber jaw syndrome
    °í¹«ÅÎÁõÈıº
  • runting syndrome
    ¼Ò¸ðÁõÈıº
  • syndrome
    ÁõÈıº
  • syndrome of crocodile tears
    ¹Ì°¢´«¹°ÁõÈıº
  • scalded skin syndrome
    È­»óÇǺÎÁõÈıº
  • sensory syndrome
    °¨°¢ÁõÈıº
  • Sertoli-cell-only syndrome
    ¹öÆÀ¼¼Æ÷ÁõÈıº, ¼¼¸£Å丮¼¼Æ÷ÁõÈıº
  • shaken baby syndrome
    Èçµé¸°¾ÆÀÌÁõÈıº
  • shock syndrome
    Ãæ°ÝÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • Ramsey-Hunt syndrome
    ·¥Áö¡©Ç寮 ÁõÈıº
  • Raynaud s syndrome
    ·¹À̳ëÁõÈıº.
  • Refsums syndrome
    ·¾¼ûÁõÈıº
  • Reiter s syndrome
    ¶óÀÌÅÍÁõÈıº.
  • Reiter syndrome
    ¶óÀÌÅÍÁõÈıº
  • Reiters syndrome
    ¶óÀÌÅÍ ÁõÈıº
  • Reye s syndrome
    ¶óÀÌÁõÈıº.
  • Rh deficiency syndrome
    Rh °áÇÌÁõÈıº
  • Rh null syndrome
    Rh ¿µ<Á¦·Î>ÁõÈıº
  • Riley Day syndrome
    ¸±¸®-µ¥ÀÌÁõÈıº.
  • Riley-Smith syndrome
    ¸±¸® ½º¹Ì½º ÁõÈıº
  • Robinsons syndrome
    ·Îºó½¼ ÁõÈıº
  • Rombergs disease = Romberg syndrome
    ·Òº£¸£Å©º´
  • Rosenthal-Kloepfer syndrome
    ·ÎÁ¨Å» Ŭ·Î¿¡ÆÛ ÁõÈıº
  • Roth-Bielschowsky syndrome
    ·ÎÆ®-ºô¼î½ºÅ°ÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • 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) .
  • camptomelic syndrome
    ±¼ÁöÁõÈıº.¼Ò¾ÆÁöü±¼°îÁõÈıº(ò¶ô÷ÏÝÍØñøý¦ÏØ) .
  • capillary leak syndrome
    ¸ð¼¼Ç÷°ü´©ÃâÁõÈıº
  • caplans syndrome
    ijÀÌÇöõ ÁõÈıº (¡­ñøý¦ÏØ)
  • carbohydrate malabsorption syndrome
    ´çÁúÈí¼öºÒ·®ÁõÈıº(ÓØòõýåâ¥ÝÕÕÞñøý¦ÏØ)
  • carcinoid syndrome
    Ä«¸£½Ã³ëÀ̵åÁõÈıº(¡­ÁõÈıº).
  • carcinoid syndrome
    Ä«¸£½Ã³ëÀ̵åÁõÈıº(¡­ñøý¦ÏØ).
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BNT Boston Naming Test; brain neurotransmitter
BPS beats per second; Behavioral Pharmacological Society; biophysical profile score; bits per second; bo...
BRA bilateral renal agenesis; bone-resorbing activity; brain-reactive antibody
BSEP brain stem evoked potential
BSER brain stem evoked response [audiometry]
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RBD right brain damaged
VBR ventricle brain ratio
MDS 7--myelodysplastic syndrome
ACS Abdominal compartment syndrome
AIDS Acquire Immune Deficiency Syndrome
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  • ¿µ¹®
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    ¼³¸í
  • Frohlich's syndrome
    ÇÁ·Ñ¸®È÷ ÁõÈıº
  • Hamman-Rich syndrome
    ÇÔ¸¸- ¸®Ä¡ ÁõÈıº, ÇØ¸Õ-¸®Ä¡ ÁõÈıº, ÇÜ¸Õ ¸®Ä¡ ÁõÈıº
    Ư¹ß¼º ¹Ì¸¸¼º °£Áú¼º Æó¿°.
  • hand shoulder syndrome
    ¼Õ-¾î±ú ÁõÈıº
  • HELLP syndrome
    HELLP ÁõÈıº
  • hematopoietic syndrome
    Á¶Ç÷ ÁõÈıº
  • hemolytic-uremic syndrome
    ¿ëÇ÷¼º ¿äµ¶ ÁõÈıº
  • Henoch Schoenlein syndrome
    Çì³ëÈ£-½¨¶óÀÎ ÁõÈıº
  • hepatocerebral syndrome
    °£ ³ú ÁõÈıº
  • hepatoovarian syndrome
    °£ ³­¼Ò ÁõÈıº
  • hepatorenal syndrome
    °£ ½Å ÁõÈıº
    °£ Áõ»ó°ú ÇÔ²² ¿äÁß¿¡ ´Ü¹é, ¿øÁÖ°¡ ³ªÅ¸³ª°í, ¿äÀÇ ºÐ·®ÀÌ °¨¼ÒÇÏ´Â »óÅÂ. °£°ú ½ÅÀåÀÌ µ¿½Ã¿¡ Àå¾Ö¸¦ ÀÏÀ¸Å°´Â ÀÏÀº ÀÓ»ó¿¡¼­ ¿¾³¯ºÎÅÍ ÀÎÁ¤µÇ¾î ¿Ô´Ù. ±× ÀÌÀ¯´Â, ù° ¼¼±ÕÀÇ °¨¿°À¸·Î ÀÎÇÑ °£ ½Å¿°, µÑ° °£ Áßµ¶, ¼Â° °£ °æº¯, ³Ý° ¹ÙÀÌ·¯½º¼ºÀ¸·Î ÀÎÇÑ °Í µîÀÌ ÀÖ´Ù.
  • heritable melanoma syndrome
    À¯Àü¼º Èæ»öÁ¾ ÁõÈıº
  • histiocytosis syndrome
    Á¶Á÷±¸Áõ ÁõÈıº
  • Holt Oram syndrome
    ȦƮ-¿À¶÷ ÁõÈıº
  • Horner's syndrome
    È£³Ê ÁõÈıº, Horner ÁõÈıº
    ÆíÃø¼º Ãൿ ¼öÁõ, ±×¸®°í ¾È¸é Å»¼öÁõÀÌ Æ¯Â¡ÀÎ ½Å°æ¼º »óÅ·μ­ º¸Åë °æºÎ ±³°¨¼º ¸¶ºñ·ÎºÎÅÍ ¹ß»ýµÈ´Ù.
  • Horton's syndrome
    Horton ÁõÈıº
    cluster headache¸¦ º¸½Ã¿À.
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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)
Book syndrome <syndrome> Premolar aplasia, hyperhidrosis, and premature canities; autosomal dominant trait.
(05 Mar 2000)
Borjeson-Forssman-Lehmann syndrome <syndrome> A condition characterised by mental deficiency, epilepsy, hypogonadism, hypometabolism, obesity, and narrow palpebral fissures; X-linked recessive inheritance.
(05 Mar 2000)
bowel bypass syndrome <syndrome> Fever, chills, malaise, and inflammatory cutaneous papules and pustules on the extremities and upper trunk, sometimes with polyarthralgia, with recurrent symptoms following bowel bypass surgery.
(05 Mar 2000)
bradytachycardia syndrome <syndrome> Alternate rapid and slow cardiac rates that may represent any rhythm disturbances in any combination usually related to sinus node disease.
Synonym: tachybradycardia syndrome.
(05 Mar 2000)
branchio-oto-renal syndrome <syndrome> An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to mondini type cochlear defect and stapes fixation.
(12 Dec 1998)
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)
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