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"mesenteric root compression 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
  • Pierre Robin syndrome
    ÇÇ¿¡¸£·Î¹ðÁõÈıº
  • placental transfusion syndrome
    ŹݼöÇ÷ÁõÈıº
  • polycystic ovarian syndrome
    ´Ù³¶³­¼ÒÁõÈıº
  • postmenopausal syndrome
    Æó°æÈÄÁõÈıº
  • post-myocardial infarction syndrome
    ½É±Ù°æ»öÈÄÁõÈıº
  • postnasal drip syndrome
    ÄÚµÚÈ帧ÁõÈıº, Èĺñ·çÁõÈıº
  • postpericardiotomy syndrome
    ½É³¶¸·Àý°³¼úÈÄÁõÈıº
  • postpolio syndrome
    ¼Ò¾Æ¸¶ºñÈÄÁõÈıº
  • Prader-Willi syndrome
    ÇÁ·¡´õ-Àª¸®ÁõÈıº
  • premenstrual syndrome
    ¿ù°æÀüÁõÈıº
  • prune-belly syndrome
    ¸»¸°´ëÃß¹èÁõÈıº
  • pulmonary overinflation syndrome
    Æó°úµµÆØÃ¢ÁõÈıº
  • paraneoplastic syndrome
    ½Å»ý¹°µþ¸²ÁõÈıº
  • Parinaud syndrome
    ÆÄ¸®³ëÁõÈıº
  • parkinsonian syndrome
    ÆÄŲ½¼ÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 18
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    ÇѱÛ
  • shaken baby syndrome
    Èçµé¸°¾ÆÀÌÁõÈıº
  • shock syndrome
    Ãæ°ÝÁõÈıº
  • short bowel syndrome
    ÀÛÀºÃ¢ÀÚÁõÈıº
  • shoulder-hand syndrome
    ¾î±ú¼ÕÁõÈıº
  • sleep apnea syndrome
    ¼ö¸é¹«È£ÈíÁõÈıº
  • sleep choking syndrome
    ¼ö¸éÁú½ÄÁõÈıº
  • somatizing syndrome
    ½ÅüȭÁõÈıº
  • stasis syndrome
    âÀÚÁ¤Ã¼ÁõÈıº
  • stiff-man syndrome
    ±ÙÀ°°­Á÷ÁõÈıº
  • stroke syndrome
    ÁßdzÁõÈıº
  • sudden infant death syndrome
    ¿µ¾Æ±Þ»çÁõÈıº
  • sudden manhood death syndrome
    ûÀå³â±Þ»çÁõÈıº
  • superior orbital fissure syndrome
    À§´«È®Æ´»õÁõÈıº
  • supine hypotensive syndrome
    ´©¿îÀÚ¼¼ÀúÇ÷¾ÐÁõÈıº
  • tabetic syndrome
    ¼Ò¸ðÁõÁõÈıº, Ÿº£½ºÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 18
  • ¿µ¹®
    ÇѱÛ
  • Vogt-Koyanagi-Harada syndrome
    º¸Å©Æ®-°í¾ß³ª±â-Ç϶ó´Ù ÁõÈıº
  • WPW syndrome
    WPWÁõÈıº, ºÎÀüµµ·ÎÁõÈıº .
  • Waardenburgs syndrome
    ¹Ù¸£µ§ºÎ¸£Å© ÁõÈıº
  • Wallenbergs syndrome
    ¹ß·»º£¸£Å©ÁõÈıº.
  • Waterhouse Friderichsen syndrome
    ¿ö¾îÅÍÇϿ콺-ÇÁ¸®µ¥¸®Å©¼¾ÁõÈıº.
  • Waterhouse-Friderichsen syndrome
    ¿öÅÍÇϿ콺-ÇÁ¸®µ¥¸¯¼¾ ÁõÈıº
  • Weber syndrome
    ¿þ¹öÁõÈıº
  • Weber-Cocayne syndrome
    ¿þ¹ö ÄÚÄÉÀÎ ÁõÈıº
  • Webers syndrome
    ¿þ¹öÁõÈıº.
  • Werners syndrome
    º£¸£³ÊÁõÈıº.
  • Wernicke Korsakoff syndrome
    º£¸£´ÏÄÉ-ÄÚ¸£»çÄÚÇÁÁõÈıº.
  • Wiskott-Aldrich syndrome
    ºñ½ºÄÚÆ®-¿Ãµå¸®Ä¡ ÁõÈıº
  • Wiskott-Aldrich syndrome
    À§½ºÄÚÆ® ¿Ãµå¸®È÷ ÁõÈıº
  • Wolff-Parkinson-White syndrome
    ¿ùÇÁÆÄŲ½¼È­ÀÌÆ® ÁõÈıº
  • Wyburn-Mason syndrome
    À§¹ø¸Å½¼ ÁõÈıº
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 18
  • ¿µ¹®
    ÇѱÛ
  • acid aspiration syndrome
    À§»ê ÈíÀÔ ÁõÈıº
  • acquired immune deficiency syndrome
    ÈÄõ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • acquired immune deficiency syndrome
    ÈÄõ¼º ¸é¿ª°áÇÌÁõÈıº(ý­ô¸àõ Øóæ¹ÌÀù¹ñøý¦ÏØ)
  • acquired immunodeficiency syndrome
    ÈÄõ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • acquired immunodeficiency syndrome
    ÈÄõ¼º¸é¿ª°áÇÌÁõ
  • acquired immunodeficiency syndrome (AIDS)
    ÈÄõ¼º¸é¿ª°áÇÌÁõ(Èıº)
  • acquired immunodeficiency syndrome(AIDS)
    ÈÄõ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • acute brain syndrome
    ±Þ¼º ³úÁõÈıº(¡­Òàñøý¦ÏØ).
  • acute fulminating meningococcemia ; Waterhouse Friderichsen syndrome
    ±Þ¼º Àü°Ý¼º ¼ö¸·±¸±Õ±ÕÇ÷Áõ.
  • acute radiation syndrome
    ±Þ¼º¹æ»ç¼±ÁõÈıº
  • acute radiation syndrome
    ±Þ¼º¹æ»ç¼±ÁõÈıº(¡­Û¯ÞÒàÊñøý¦ÏØ)
  • adherence syndrome, Johnson
    ÁÔ½¼À¯ÂøÁõÈıº
  • adhesive syndrome
    À¯ÂøÁõÈıº
  • adrenal cortex,cushings syndrome
    Äí½ÌÁõÈıº(¡­ñøý¦ÏØ)
  • adrenal virilizing syndrome
    ºÎ½Å¼º ³²¼ºÈ­ ÁõÈıº(¡­ñøý¦ÏØ).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 18
PS pacemaker syndrome; paired stimulation; paradoxical sleep; paraspinal; parasympathetic; Parkinson sy...
SS disulfide; sacrosciatic; saline soak; saline solution; saliva sample; saliva substitute; Salmonella-...
SSS scalded skin syndrome; secondary Sjogren syndrome; sick sinus syndrome; specific soluble substance; ...
TS Takayasu syndrome; Tay-Sachs; temperature sensitivity; temperature, skin; temporal stem; tensile str...
CC   1) Chief Complaint; ÁÖ¼Ò(ñ«áÍ), ÁÖµÈ È£¼Ò(ºÒÆò)
  2) Closing Capacity
  ...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 18
BWS Beckwith Wiedemann Syndrome
BS Behcet's Syndrome
BSS Bernard Soulier Syndrome
BPES Blepharophimosis Ptosis Epicanthus inversus Syndrome
BS Bloom Syndrome
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  • 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¿°.
  • 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
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 18
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)
Biemond syndrome <syndrome> Iris coloboma, mental retardation, obesity, hypogenitalism, and postaxial polydactyly; a recessive inheritance disorder resembling Laurence-Moon and Bardet-Biedel syndrome's.
(05 Mar 2000)
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