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  • ¿µ¹®
    ÇѱÛ
  • 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
  • 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
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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
  • PANSS=Positive and Negative Syndrome Scale
    ¾ç¼º À½¼º ÁõÈıº ôµµ
  • PIE syndrome
    È£»ê±¸¼º Æóħ½À ÁõÈıº
  • PMS(postmenopausal syndrome)
    Æó°æ±â ÁõÈıº
  • PMS(premenstrual syndrome)
    ¿ù°æÀü ÁõÈıº
  • PMS.see premenstrual syndrome
    ¿ù°æÀüÁßÈıº(êÅÌèîññøý¦ÏØ)
  • Papillon-Lefervre syndrome
    ÆÄÇÇ¿ë-¸£Æäºê¸£ ÁõÈıº
  • Parinauds oculonoduler syndrome
    ÆÄ¸®³ë¾È ¸²ÇÁÀý ÁõÈıº.
  • Parinauds syndrome
    ÆÄ¸®³ëµåÁõÈıº
  • Peutz-Jeghers syndrome
    Ç»Ã÷Á¦°Å½ºÁõÈıº.
  • Peutz-Jeghers syndrome
    Æ÷ÀÌÃ÷-¿¹°ÅÁõÈıº.
  • Pickwickian syndrome
    ÇÇÅ©À§Å© ÁõÈıº
  • Plummer Vinson syndrome
    Ç÷¯¸Ó-ºó¼ÕÁõÈıº
  • Plummer-Vinson syndrome
    Ç÷¯¸Óºó½¼ÁõÈıº.
  • Poland syndrome
    Æú¶õµåÁõÈıº
  • Posner-Schlossman syndrome=>glaucomatocyclitic crisis
    Æ÷½º³Ê-½¯·Î½º¸¸ ÁõÈıº
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  • ¿µ¹®
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  • third aortic arch
    ¼Â°´ëµ¿¸ÆÈ°
  • third arch
    ¼Â°ÀεαÁÀÌ
  • third arch (iii)
    ¼Â°±ÁÀÌ
  • transverse arch of foot
    ¹ß¹Ù´Ú°¡·Î? ȾÁ·?üôðëÏá).
  • vertebral arch
    ôÃß? Ãß?õÐÏá).
  • vertebral arch
    ôÃß»À°í¸®
  • visceral arch
    (³»)Àå?Ò®íôÏá).
  • visceral cranium =Brachial arch
    ³»Àå(Ò®íô)µÎ°³°ñ, ¾Æ°¡¹Ìµï
  • zygomatic arch
    Çù°ñ±Ã, °ü°ñ±Ã
  • zygomatic arch
    °ü°ñ? Çù°ñ?úúÍéÏá).
  • zygomatic arch
    ±¤´ëȰ
  • 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
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
NI-NXII first to twelfth cranial nerves
P1, P-one first parental generation
PI first meiotic prophase; isoelectric point; pacing impulse; package insert; pancreatic insufficiency;...
S1-S5 first to fifth sacral nerves
S1-S4 first to fourth heart sounds
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CCHS Congenital central hypoventilation syndrome
CS Cowden syndrome
CS Cushing syndrome
CVS Cyclic vomiting syndrome
DSS Dejerine-Sottas Syndrome
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  • 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
  • excited skin syndrome
    ÈïºÐ¼º ÇǺΠÁõÈıº
  • extrapyramidal syndrome
    Ãßü¿Ü·Î ÁõÈıº
  • facio-auriculo-vertebral syndrome
    ¾È¸é-ÀÌ-ôÃß ÁõÈıº
  • Fanconi's syndrome
    Fanconi ÁõÈıº
    1. Ç÷±¸°¨¼ÒÁõ, °ñ¼öÀÇ Çü¼º ºÎÀü, ¸á¶ó´Ñ Ä§Âø¿¡ ÀÇÇÑ ÇǺÎÀÇ »ö¼Ò¹Ý, ±Ù°ñ°Ý°è¿Í ºñ´¢ »ý½Ä°èÀÇ ¼±Ãµ¼º ÀÌ»óÀ» Ư¡À¸·Î ÇÏ´Â À¯Àü¼º Áúȯ. 2. ±ÙÀ§ ¼¼´¢°üÀÇ ±â´ÉÀå¾Ö·Î ÀÎÇÑ ÀÏ·ÃÀÇ ÁúȯÀ» °¡¸£Å°´Â ¿ë¾î. °íÀλ괢, ´ç´¢, Àü¾Æ¹Ì³ë»ê´¢, Áßź»ê¿°°ú ¼öºÐÀÇ ¼Õ½ÇÀÌ ÀÖ´Ù.
  • fat embolism syndrome
    Áö¹æ »öÀü ÁõÈıº
    Áö¹æ ¼ººÐÀÌ ´ëºÎºÐÀΠȲ»ö °ñ¼ö·Î µÈ °ñÀÇ °ñÀý ¶Ç´Â Áö¹æ Á¶Á÷ÀÇ ½ÉÇÑ ¿Ü»ó ÈÄ¿¡ Á¡ÁøÀû Æó ºÎÀüÁõ, Á¤½Å·Â ÀúÇÏ¿Í ½Å ºÎÀüÁõÀ» ÃÊ·¡ÇÏ´Â °ÍÀ» ¸»ÇÑ´Ù. ÀÌ´Â ÆÄ¿­µÈ Ç÷°ü ¼ÓÀ¸·Î ¹«¼öÇÑ Áö¹æ±¸°¡ µé¾î°¡ ¿©·¯ Àå±â¿¡ ºÐÆ÷ÇÑ Ç÷°ü¿¡ »öÀüÁõÀ» ¾ß±âÇÔÀ¸·Î½á ÀϾ´Ù. ÀϹÝÀûÀ¸·Î º´ÀηÐÀº º¹ÇÕÀûÀÌ´Ù. ÀÏ´Ü ÀÌ ÁõÈıºÀÌ ¹ß»ýÇÏ¸é ¸Å¿ì À§µ¶ÇÏ¿© ´ë·« 10-15%ÀÇ »ç¸Á·üÀ» ³ªÅ¸³½´Ù.
  • 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¿°.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
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)
Besnier-Boeck-Schaumann syndrome <disease> Disease of unknown aetiology in which there are chronic inflammatory granulomatous lesions in lymph nodes and other organs.
(18 Nov 1997)
Beuren syndrome <syndrome> Supravalvular aortic stenosis with multiple areas of peripheral pulmonary arterial stenosis, mental retardation, and dental anomalies.
(05 Mar 2000)
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