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"joint hypermobility 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
  • runting syndrome
    ¼Ò¸ðÁõÈıº, ¿Ö¼ÒÁõÈıº
  • Raynaud¡¯s syndrome
    ·¹À̳ëÁõÈıº
  • radial tunnel syndrome
    ³ëÂʱ¼ÁõÈıº, ¿äÃø±¼ÁõÈıº
  • refeeding syndrome
    ¿µ¾çÀç°³ÁõÈıº, ±Þ½ÄÀç°³ÁõÈıº
  • Reiter¡¯s syndrome
    ¶óÀÌÅÍÁõÈıº
  • respiratory distress syndrome
    È£Èí°ï¶õÁõÈıº
  • radicular syndrome
    ½Å°æ»Ñ¸®ÁõÈıº, ½Å°æ±ÙÁõÈıº
  • retraction syndrome
    ¾È±¸ÈÄÅðÁõÈıº
  • scalded skin syndrome
    È­»óÇǺÎÁõÈıº
  • staphylococcal scalded skin syndrome
    Æ÷µµ¾Ë±Õ¼º¿­»óÇǺÎÁõÈıº, Æ÷µµ±¸±Õ¼º¿­»óÇǺÎÁõÈıº
  • stasis syndrome
    âÀÚÁ¤Ã¼ÁõÈıº, ÀåÁ¤Ã¼ÁõÈıº
  • Steele-Richardson-Olszewski syndrome
    ½ºÆ¿-¸®Ã³µå½¼-¿Ã½ºÁ¦ºê½ºÅ°ÁõÈıº
  • Scheie syndrome
    »þÀÌ¿¡ÁõÈıº
  • Stevens-Johnson syndrome
    ½ºÆ¼ºì½º-Á¸½¼ÁõÈıº
  • stiff-man syndrome
    °­Á÷ÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 19
  • ¿µ¹®
    ÇѱÛ
  • tarsal tunnel syndrome
    ¹ß¸ñ±¼ÁõÈıº, Á·±Ù°üÁõÈıº
  • testicular feminization syndrome
    °íȯ¿©¼ºÈ­ÁõÈıº
  • thalamic syndrome
    ½Ã»óÁõÈıÙ
  • time zone change syndrome
    (¢¡jet lag syndrome) ºñÇà½ÃÂ÷ÁõÈıº
  • toxic shock syndrome
    µ¶¼ÒÃæ°ÝÁõÈıº
  • transurethral resection syndrome
    °æ¿äµµÀýÁ¦ÈÄÁõÈıº
  • trisomy 18 syndrome
    18¼¼¿°»öüÁõÈıº
  • ulnar tunnel syndrome
    ÀÚ»À±¼ÁõÈıº, ô°ñ°üÁõÈıº
  • unknown genesis syndrome
    ¹ß»ý¹Ì»óÁõÈıº
  • vanishing testes syndrome
    °íȯ¼Ò¸êÁõÈıº
  • velocardiofacial syndrome
    ÀÔõÀå½ÉÀå¾ó±¼ÁõÈıº
  • virilizing syndrome
    ³²¼ºÈ­ÁõÈıº
  • vitreouswick wick syndrome
    À¯¸®Ã¼½ÉÁöÁõÈıº
  • wasting syndrome
    ¼Ò¸ðÁõÈıº
  • withdrawal syndrome
    ±Ý´ÜÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • 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
  • X-linked lymphoproliferative syndrome
    ¼º¿°»öü ¿¬°ü ¸²ÇÁÁõ½Ä ÁõÈıº
  • XXY syndrome
    XXYÁõÈıº.
  • XXYY syndrome
    XXYYÁõÈıº.
  • Zieves syndrome
    ÁöºêÁõÈıº
  • Zollinger-Ellison syndrome
    Á¹¸µ°Å ¿¤¸®¼Õ ÁõÈıº
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  • ¿µ¹®
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  • anterior chamber cleavage syndrome
    Àü¹æ(°¢)ºÐ¸®ºÎÀüÁõÈıº
  • anterior choroidal artery occlusion syndrome
    Àü¸Æ¶ôÃѵ¿¸Æ Æó¼âÁõÈıº.
  • anterior cornual syndrome
    Àü°¢ÁõÈıº(îñÊÇñøý¦ÏØ).
  • anterior scalene syndrome
    Àü»ç°¢±ÙÁõÈıº(îñÞØÊÇÐÉñøý¦ÏØ).
  • anterior spinal artery syndrome
    Àüô¼öµ¿¸ÆÁõÈıº(¡­ñøý¦ÏØ).
  • anterior spinal syndrome
    Àü»èÁõÈıº(¡­ñøý¦ÏØ).
  • anterior tibial syndrome
    Àü°æ°ñÁõÈıº
  • anterolateral syndrome
    ô¼öÀüÃø°¢ÁõÈıº(ô±âÐîñö°ÊÇñøý¦ÏØ).
  • antibody deficiency syndrome
    Ç×ü°áÇÌÁõÈıº(ù÷ô÷ÌÀù¹ñøý¦ÏØ).
  • anticardiolipin syndrome
    Ç×Ä«¸£µð¿Ã¸®ÇÉÁõÈıº
  • anticardiolipin syndrome
    Ç×Ä«µð¿À¸®ÇÉÁõÈıº
  • antiphospholipid syndrome
    Ç×ÀÎÁöÁúÁõÈıº
  • anxiety syndrome
    ºÒ¾ÈÁõÈıº(¡­ñøý¦ÏØ).
  • aortic arch syndrome
    ´ëµ¿¸Æ±ÃÁõÈıº(¡­ñøý¦ÏØ).
  • aortic arch syndrome
    ´ëµ¿¸Æ±Ã ÁõÈıº(¡­Ïáñøý¦ÏØ)
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MPJ metacarpophalangeal joint
MTC mass transfer coefficient; maximum tolerated concentration; maximum toxic concentration; medical tes...
MTPJ metatarsophalangeal joint
NJPC National Joint Practice Commission
PIPJ proximal interphalangeal joint
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 19
DSPS Delayed Sleep Phase Syndrome
DHF/DSS Dengue Haemorrhagic Fever/Dengue Shock Syndrome
DSS Dengue Shock Syndrome
DDS Denys Drash syndrome
DGS Di George syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 19
  • ¿µ¹®
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    ¼³¸í
  • 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
  • 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.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 19
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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