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  • ¿µ¹®
    ÇѱÛ
  • 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
  • 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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    ÇѱÛ
  • postpartum mood syndrome
    »êÈıâºÐÁõÈıº
  • premenstrual syndrome
    ¿ù°æÀüÁõÈıº
  • presbyophrenia syndrome
    ³ëÀÎÄ¡¸Å
  • prodromal radiation syndrome
    Á¶Áü¹æ»ç¼±ÁõÈıº
  • prune-belly syndrome
    ¸»¸°´ëÃßÁõÈıº
  • psychomotor syndrome
    Á¤½Å¿îµ¿ÁõÈıº
  • 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
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  • ¿µ¹®
    ÇѱÛ
  • 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
  • Rubinstein-Taybi syndrome
    ·çºó½ºÅ¸ÀÎ Å×À̺ñ ÁõÈıº
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  • ¿µ¹®
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  • 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).
  • auriculotemporal syndrome
    À̰³ÃøµÎ ÁõÈıº(ì¼Ë¿ö°Ôé ñøý¦ÏØ)
  • bantis syndrome
    ¹ÝƼÁõÈıº(¡­ñøý¦ÏØ)
  • bartters syndrome
    ¹ÙÅÍ ÁõÈıº(¡­ñøý¦ÏØ)
  • basal cell nevus syndrome
    ±âÀú¼¼Æ÷¸ð¹ÝÁõÈıº(¡­Ù½Úèñøý¦ÏØ).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 15
HHH Syndrome Hyperamnonemia-Hyperornithinemia-Homocitrullinemia Syndrome
LAMB Syndrome Lentigines, Atrial myxoma, Blue nevi Syndrome
LGL Syndrome Lown-Ganong-Levine Syndrome
LUF syndrome Lutenized Unruptured Follicle syndrome
MAS Meconium Aspiration Syndrome; ź¯(¾ç¼ö)ÈíÀÎÁõÈıº
  = Massive Aspiration Syndrome; ¾ç¼ö ´ë·® ÈíÀÎ ÁõÈÄ...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 15
DILS Diffuse Infiltrative Lymphocytosis Syndrome
DIC Disseminated intravascular coagulation syndrome
DS Down Syndrome
DRS Duane retraction syndrome
DJS Dubin Johnson Syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 15
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    ¼³¸í
  • 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.
  • Hurler-Scheie syndrome
    Çæ·¯-»þÀÌ¿¡ ÁõÈıº
  • Hutchinson's syndrome
    ÇãÄ£½¼ ÁõÈıº
    °£Áú °¢¸·¿°, ¹Ì·Î Áúȯ, ÇãÄ£½¼ Ä¡¾ÆÀÇ º¹ÇÕÀ¸·Î ¼±Ãµ ¸Åµ¶¿¡¼­ º¼ ¼ö ÀÖ´Ù. ¼±Ãµ¼º ¸Åµ¶ÀÇ Áõ»óÀ¸·Î ÇãÄ£½¼ 3ÁÖÁõÀ¸·Î Áø´ÜÇÒ ¼ö ÀÖ´Ù. ¸Åµ¶Àº 1Â÷, 2Â÷, 3Â÷ÀÇ ´Ü°è¸¦ º¸À̸ç À¯Àü¼ºÀ» ¶ì°í ÀÖ´Ù.
  • hyperimmunoglobulin E syndrome
    °ú¸é¿ª ±Û·ÎºÒ¸° E ÁõÈıº
  • hyperkinetic heart syndrome
    °ú¿îµ¿¼º ½ÉÁõÈÄ, °ú¿îµ¿¼º ½ÉÁõÈıº
  • hypermobility syndrome
    °ú¿îµ¿ ÁõÈıº
  • hyperstimulation syndrome
    °úÀÚ±Ø ÁõÈıº
  • hyperviscosity syndrome
    °íÁ¡µµ ÁõÈıº
    °ñ¼öÁ¾ ´Ü¹éÀÌ °ú´ÙÇÏ°Ô »ý¼ºµÈ °ÍÀÌ ÀÀÁýµÇ¾î ³ªÅ¸³­´Ù. ´Ù¹ß¼º °ñ¼öÁ¾ ȯÀÚÀÇ ¾à 7%¿¡¼­ º¼ ¼ö ÀÖ´Ù.
  • hypogenetic lung syndrome
    Àú¹ß»ý Æó ÁõÈıº
  • hypoglossia hypodactyly syndrome
    ¼³Áö Çü¼º ºÎÀü ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 15
battered spouse syndrome <syndrome> Physical, psychological, and emotional injuries in a person subjected to abuse by a spouse or domestic partner; usually associated with alcoholism in the abusing spouse.
(05 Mar 2000)
Bauer's syndrome <syndrome> Aortitis and aortic endocarditis as a little recognised manifestation of rheumatoid arthritis.
(05 Mar 2000)
Bazex's syndrome <syndrome> Erythematous to plum-coloured scaly acral skin lesions, paronychia, and nail dysplasia; associated with cancer of the upper respiratory or upper alimentary tract.
Synonym: paraneoplastic acrokeratosis.
(05 Mar 2000)
Beckwith syndrome <syndrome> This syndrome, of unknown cause, is characterised by a group of the following findings: large tongue, organ enlargement (visceromegaly), large body size, umbilical hernia and neonatal hypoglycaemia. Evidence suggests a genetic lesion. Birth weight is often more than 8 pounds. Complications include Wilm's tumour, seizures, aspiration and hypoglycaemia.
(27 Sep 1997)
Beckwith-Wiedemann syndrome <syndrome> This syndrome, of unknown cause, is characterised by a group of the following findings: large tongue, organ enlargement (visceromegaly), large body size, umbilical hernia and neonatal hypoglycaemia. Evidence suggests a genetic lesion. Birth weight is often more than 8 pounds. Complications include Wilm's tumour, seizures, aspiration and hypoglycaemia.
(27 Sep 1997)
Behcet's syndrome <syndrome> A multisystem, chronic recurrent disease characterised by ulceration in the mouth and genitalia, iritis, uveitis, arthritis and thrombophlebitis. Often treated with immunosuppressive therapy (corticosteroids, chlorambucil).
(27 Sep 1997)
Behr's syndrome <syndrome> Adult or presenile form of heredomacular degeneration.
Synonym: Behr's disease.
(05 Mar 2000)
Benedikt's syndrome <syndrome> Hemiplegia with clonic spasm or tremor and oculomotor paralysis on the opposite side.
(05 Mar 2000)
Beradinelli's syndrome <syndrome> The clinical findings of accelerated growth, lipodystrophy with muscular hypertrophy, hepatomegaly and lipaemia.
(27 Sep 1997)
Bernard-Horner syndrome <syndrome> A nerve condition which involves a dropping eyelid (ptosis), constricted pupil, enophthalmos and lack of sweating on one side of the face. Often seen in association with injury (for example neck fracture, penetrating injury) to the cervical sympathetic nerve trunk in the neck or a Pancoast tumour involving both the upper and lower brachial plexus.
(29 Sep 1997)
Bernard-Sergent syndrome Severe adrenocortical insufficiency when an intercurrent illness or trauma causes an increased demand for adrenocortical hormones in a patient with adrenal insufficiency due to disease or use of relatively large amounts of similar hormones as therapy; characterised by nausea, vomiting, hypotension, and frequently hyperthemia, hyponatraemia, hyperkalaemia, and hypoglycaemia; can be fatal if untreated.
Synonym: addisonian crisis, adrenal crisis, Bernard-Sergent syndrome.
(05 Mar 2000)
Bernard Soulier syndrome <haematology, syndrome> A congenital disorder where the platelets lack receptors which allow them to adhere to the walls of blood vessels. The genetic deficiency in platelet membrane glycoprotein Ib allows platelets to aggregate normally (c.f. Glanzmann's thrombasthenia) but they do not stick to collagen of sub endothelial basement membrane. The net result is a platelet function disorder that causes a prolonged bleeding time.
Symptoms include nosebleeds, easy bruising, heavy menstrual periods, bleeding gums and increased post-operative bleeding. Avoidance of aspirin, anti-inflammatories or any other agents which can cause bleeding is critical.
(06 Oct 1997)
bernard syndrome <syndrome> A complex of abnormal findings, namely sinking in of one eyeball, ipsilateral ptosis (drooping of the upper eyelid on the same side) and miosis (constriction of the pupil of that eye) together with anhidosis (lack of sweating) and flushing of the affected side of the face.
Due to paralysis of certain nerves (specifically, the cervical sympathetic nerves). Also called Horner-Bernard syndrome, Bernard-Horner syndrome and Horner's ptosis, but best known today as Horner syndrome.
(12 Dec 1998)
Bernhardt-Roth syndrome <symptom> A tingling, formication, itching, and other forms of paresthesia in the outer side of the lower part of the thigh in the area of distribution of the lateral femoral cutaneous nerve; there may be pain, but the skin is usually hypesthetic to the touch.
Synonym: Bernhardt's disease, Bernhardt-Roth syndrome, Roth's disease, Roth-Bernhardt disease.
(21 Sep 2000)
Bernheim's syndrome <syndrome> Systemic congestion resembling the consequences of right heart failure (enlarged liver, distended neck veins, and oedema) without pulmonary congestion in subjects with left ventricular enlargement from any cause.
A reduction in the size of the right ventricular cavity is found by contrast imaging or echocardiography or at postmortem due to encroachment by the hypertrophied or aneurysmal ventricular septum.
(14 Aug 2000)
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