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"multiple lipoma 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
  • McCune-Albright syndrome
    ¸ÆÄï-¿Ãºê¶óÀÌÆ®ÁõÈıº
  • meconium plug syndrome
    ꝏ¶°³ÁõÈıº
  • megacystis-megaureter syndrome
    °Å´ë¹æ±¤°Å´ë¿ä°üÁõÈıº
  • Meigs¡¯ syndrome
    ¸ÞÀ̱×ÁõÈıº
  • nephritic syndrome
    ÄáÆÏ¿°ÁõÈıº, ½ÅÀå¿°ÁõÈıº
  • nephrotic syndrome
    ÄáÆÏÁõÈıº, ½ÅÁõÈıº
  • neuroleptic malignant syndrome
    ½Å°æÀÌ¿ÏÁ¦¾Ç¼ºÁõÈıº
  • neurovascular syndrome
    ½Å°æÇ÷°üÁõÈıº
  • Noonan¡¯s syndrome
    ´©³­ÁõÈıº
  • 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 brain syndrome
    ±âÁú¼º³úÁõÈıº
  • organic mental syndrome
    ±âÁú¼ºÁ¤½ÅÁõÈıº
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    ÇѱÛ
  • otocraniocephalic syndrome
    ±Í¸Ó¸®ÁõÈıº, À̵ΰ³ÁõÈıº
  • overlap syndrome
    °ãħÁõÈıº, ÁßøÁõÈıº
  • overwear syndrome
    °úµµÂø¿ëÁõÈıº
  • preleukemia myelodysplastic syndrome
    °ñ¼öÇü¼ºÀÌ»óÁõÈıº
  • pancoast syndrome
    ÆÇÄÚ½ºÆ®ÁõÈıº
  • peeling skin syndrome
    ÇǺιڸ®ÁõÈıº
  • phantom lover syndrome
    ȯ»ó¿¬ÀÎÁõÈıº
  • pluriglandular syndrome
    ¹µ»ùÁõÈıº, ¿©·¯»ùÁõÈıº
  • positive and negative syndrome
    ¾ç¼ºÀ½¼ºÁõÈıº
  • post-infarction syndrome
    °æ»öÈÄÁõÈıº
  • postelectric shock syndrome
    Àü±âÃæ°ÝÈÄÁõÈıº
  • postencephalitic behavioral syndrome
    ³ú¿°ÈÄÇൿÁõÈıº
  • postmenopausal syndrome
    Æó°æÈÄÁõÈıº
  • postpartum mood syndrome
    »êÈıâºÐÁõÈıº
  • premenstrual syndrome
    ¿ù°æÀüÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 15
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  • Sj grens syndrome
    ¼î±×·»ÁõÈıº
  • Sjo gren s syndrome
    ¼î±×·»ÁõÈıº.
  • Sjogrens syndrome
    ¼î±×·»ÁõÈıº
  • Stein Leventhal syndrome
    ½ºÅ¸ÀÎ-·¹º¥Å»ÁõÈıº.
  • Stevens-Johnson syndrome
    ½ºÆ¼ºì½º-Á¸½¼ÁõÈıº
  • Stewart-Treves syndrome
    ½ºÆ©¾îÆ® Æ®¸®ºê½º ÁõÈıº
  • Stickler syndrome
    ½ºÆ¼Å¬·¯ ÁõÈıº.
  • Stipples syndrome
    ½ºÆ¼Çà ÁõÈıº.
  • Sturge Weber syndrome
    ½ºÅÍÁö-¿þ¹öÁõÈıº.
  • Tietzes syndrome
    ƼÂÅÁõÈıº.
  • Turners syndrome
    ÅÍ³Ê ÁõÈıº
  • Ushers syndrome
    ¾Æ¼ÅÁõÈıº
  • V-syndrome
    VÁõÈıº
  • V-syndrome
    V ÁõÈıº
  • Vogt-Koyanagi syndrome
    Æ÷±×Æ® °í¾ß³ª±â ÁõÈıº
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  • aortitis syndrome
    ´ëµ¿¸Æ¿°ÁõÈıº(¡­æúñøý¦ÏØ).
  • aortitis syndrome
    ´ëµ¿¸Æ¿° ÁõÈıº(¡­ñøý¦ÏØ)
  • apallic syndrome
    ¹«½ÉÁõÈıº(Ùíãýñøý¦ÏØ)
  • apathetic-akinetic syndrome
    ¹«°¨µ¿-¹«µ¿ÀÛ ÁõÈıº
  • aphasic and apraxic syndrome
    ½Ç¾î½ÇÇàÁõÈıº(ã÷åÞãùú¼ñøý¦ÏØ).
  • aqueous mis-direction syndrome
    ¹æ¼öÈ帧ÀÌ»óÁõÈıº
  • ards(adult respiratory disress syndrome)
    ARDS(¼ºÀÎÈ£Èí°ï¶õÁõÈıº)(à÷ìÑû¼ýåÍÝÑññøý¦ÏØ)
  • arthritis-dermatitis syndrome
    °üÀý¿°-ÇǺο° ÁõÈıº
  • ashermans syndrome
    ¾Æ¼Å¸¸ ÁõÈıº
  • asphyctic syndrome
    Áú½ÄÁõÈıº.
  • atomic bomb syndrome
    ¿ø(ÀÚ)Æø(ź)ÁõÈıº.
  • atypical or mixed organic brain syndrome
    ºñÁ¤Çü ³»Áö È¥ÇÕÇü ±âÁú¼º ³úÁõÈıº
  • atypical schizophrenic syndrome
    ºñÁ¤Çü Á¤½ÅºÐ¿­¼º ÁõÈıº
  • auriculotemporal nerve syndrome
    À̰³ÃøµÎ½Å°æÁõÈıº.
  • auriculotemporal syndrome
    À̰³ÃøµÎÁõÈıº(¡­ñøý¦ÏØ).
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HPS Hantavirus pulmonary syndrome; hematoxylin, phloxin, and saffron; Hermansky-Pudlak syndrome; high-pr...
IAS immunosuppressive acidic substance; infant apnea syndrome; insulin autoimmune syndrome; interatrial ...
LAS laboratory automation system; lateral amyotrophic sclerosis; laxative abuse syndrome; left anterior-...
LGS Langer-Giedion syndrome; Lennox-Gastaut syndrome; limb girdle syndrome
MPS meconium plug syndrome; medial premotor system; Member of the Pharmaceutical Society; microbial prof...
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MOM multiple of the median
MOM multiple of the normal median
M-PHD multiple pituitary hormone deficiencies
MPCR multiple polymerase chain reaction
RR MS relapsing remitting multiple sclerosis
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  • Felty's syndrome
    ÆçƼ ÁõÈıº
    À§Ã༺ ´Ù°üÀý¿°. ºñÁ¾. ¹éÇ÷±¸ ¹× Ç÷¼ÒÆÇ °¨¼ÒÁõ, Àú»ö¼ÒÁõ¼º ºóÇ÷, ¹ß¿­ ÇǺΠ»ö¼Ò Ä§Âø.
  • fetal distress syndrome
    ÅÂ¾Æ °ï¶õ ÁõÈıº
  • Fiessinger-Rendu syndrome
    Fiessinger-Rendu ÁõÈıº
  • fragile x syndrome
    ÇÁ·¡ÀÚÀÏ ¿§½º ÁõÈıº
    À¯ÀüÀÚ X ¿°»öüÀÇ Àå¿Ï
  • 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
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 15
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)
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)
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