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"capsular block 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
  • Ganser syndrome
    °£ÀúÁõÈıº
  • hypereosinophilic syndrome
    °ú´ÙÈ£»ê±¸ÁõÈıº
  • hyper-IgM syndrome
    °í¸é¿ª±Û·ÎºÒ¸°MÁõÈıº
  • hyperimmunoglobulin E syndrome
    °í¸é¿ª±Û·ÎºÒ¸°EÁõÈıº
  • hyperstimulation syndrome
    °ú´ÙÀÚ±ØÁõÈıº
  • hyperventilation syndrome
    °ú´Ùȯ±âÁõÈıº
  • hyperviscosity syndrome
    °ú´ÙÁ¡¼ºÁõÈıº
  • hypoventilation syndrome
    Àúȯ±âÁõÈıº
  • hemolytic uremic syndrome
    ¿ëÇ÷¿äµ¶ÁõÈıº
  • hemopleuropneumonic syndrome
    Ç÷¾×°¡½¿¸·Æó·ÅÁõÈıº, Ç÷¾×È丷Æó·ÅÁõÈıº
  • Hallervorden-Spatz syndrome
    ÇÒ·¯º¸¸£µ§-½´ÆÄÃ÷ÁõÈıº
  • hemorrhagic fever with renal syndrome
    ÃâÇ÷¿­ÄáÆÏÁõÈıº, ÃâÇ÷¿­½ÅÁõÈıº
  • hepatorenal syndrome
    °£ÄáÆÏÁõÈıº
  • hand-foot syndrome
    ¼Õ¹ßÁõÈıº
  • hantavirus pulmonary syndrome
    ÇÑŸ¹ÙÀÌ·¯½ºÆóÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • hyperstimulation syndrome
    °ú´ÙÀÚ±ØÁõÈıº
  • hyperventilation syndrome
    °ú´ÙÈ£ÈíÁõÈıº
  • hyperviscosity syndrome
    °ú´ÙÁ¡¼ºÁõÈıº
  • hypoventilation syndrome
    È£ÈíÀúÇÏÁõÈıº
  • idiopathic cramp syndrome
    Ư¹ß°æ·ÃÁõÈıº
  • idiopathic respiratory distress syndrome
    Ư¹ßÈ£Èí°ï¶õÁõÈıº
  • immersion foot syndrome
    ħ¼ö¹ßÁõÈıº, ¹ß´ã±ÝÁõÈıº
  • immune amnesia syndrome
    ¸é¿ª±â¾ï»ó½ÇÁõÈıº
  • immunoproliferative syndrome
    ¸é¿ª¼¼Æ÷Áõ½ÄÁõÈıº
  • impingement syndrome
    ºÎµúÈûÁõÈıº
  • infantile stiff skin syndrome
    ¿µ¾ÆÇǺΰæÁ÷ÁõÈıº
  • interosseous nerve syndrome
    »À»çÀ̽ŰæÁõÈıº, °ñ°£½Å°æÁõÈıº
  • intersection syndrome
    ±³Â÷ÁõÈıº
  • intracerebral steal syndrome
    ³ú³»Ç÷·ùÀúÇÏÁõÈıº
  • irritable bowel syndrome
    °ú¹Î´ëÀåÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 12
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    ÇѱÛ
  • Hunters syndrome => mucopolysaccharidosis
    ÇåÅÍ ÁõÈıº
  • Hurler syndrome
    Èĸ¦·¯ÁõÈıº
  • Hurlers syndrome => mucopolysaccharidosis
    Èĸ¦·¯ ÁõÈıº
  • Hutchinson Gilford syndrome
    ÇãÄ£½¼-±æÆ÷¿ÀµåÁõÈıº.
  • Hutchinson-Gilford syndrome => progeria
    ÇãÄ£½¼-±æÆ÷µå ÁõÈıº
  • Imerslund-Gra sbeck syndrome
    À̸ӽ½·éµå-±×·¹½ºº£Å© ÁõÈıº
  • Irvine-Gass syndrome
    ¾î¹ÙÀÎ-°¡½º ÁõÈıº
  • Job-Buckley syndrome
    Á¼-¹öŬ¸® ÁõÈıº
  • Kallmann syndrome
    Ä®¸¸ÁõÈıº
  • Kanners syndrome
    Ä­³ÊÁõÈıº(~ñøý¦ÏØ)
  • Kassabach-Meritt syndrome
    Ä«»ç¹ÙÇÏ-¸Þ¸®Æ® ÁõÈıº
  • Kawasaki disease => mucocutaneous lymph node syndrome
    °¡¿Í»çŰ º´
  • Kernohan s syndrome
    Ä¿³ëÇÑÁõÈıº.
  • Kinky hair syndrome
    ŲŰÇì¾îÁõÈıº
  • Klinefelter s syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº.
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    ÇѱÛ
  • paravertebral block
    ôÃßÁÖÀ§Â÷´Ü(ô±õÐñ²êÌó´Ó¨).
  • paravertebral lumbar sympathetic ganglion block
    ¿äÃßÁÖÀ§±³°¨½Å°æÀýÂ÷´Ü.
  • paravertebral thoracic somatic nerve block
    ÈäÃßÁÖÀ§Ã¼¼º ½Å°æÂ÷´Ü, ôÃßÁÖ À§ÈäºÎü¼º ½Å°æÂ÷´Ü.
  • partial block
    ºÒ¿ÏÀüÂ÷´Ü.
  • penile block
    À½°æÂ÷´Ü.
  • penis block
    À½°æÂ÷´Ü(¡­ó´Ó¨).
  • peridural block
    °æ¸·ÁÖÀ§(¿Ü)Â÷´Ü(¡­ó´Ó¨).
  • periinfarction block
    °æ»öÁÖÀ§Â÷´Ü(ÌÛßáñ²êÌó´Ó¨).
  • peripheral nerve block
    ¸»ÃʽŰæÂ÷´Ü.
  • phase I block
    Á¦1»óÂ÷´Ü.
  • phenol block
    Æä³îÂ÷´Ü.
  • phrenic nerve block
    Ⱦ°Ý½Å°æÂ÷´Ü, Ⱦ°Ý¸·½Å°æÂ÷´Ü.
  • plexus block
    ½Å°æÃÑÂ÷´Ü.
  • point under block
    ºí·ÏÇÏÁöÁ¡
  • protective block
    º¸È£ºí·Ï.
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 12
IBBBB incomplete bilateral bundle branch block
ILBBB incomplete left bundle branch block
IRBBB incomplete right bundle branch block
IVB intraventricular block; intravitrial blood
LAFB left anterior fascicular block
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 12
BS Behcet's Syndrome
BSS Bernard Soulier Syndrome
BPES Blepharophimosis Ptosis Epicanthus inversus Syndrome
BS Bloom Syndrome
BRBNS Blue Rubber Bleb Nevus Syndrome
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  • carpal tunnel syndrome
    ¼ö±Ù°ü ÁõÈıº, ÆÈ¸ñ ÅͳΠÁõÈıº
    1. ¼Õ°¡¶ôÀ» Á¶ÀýÇÏ´Â Àδ븦 µÑ·¯½Î´Â Ȱ¸·ÀÌ ÀÚ±ØÀ» ¹Þ°Å³ª ¿°ÁõÀÌ »ý±ä °Í. ÆÈ¸ñ ÅͳΠÁõÈıºÀº ¼ÕÀ¸·Î ÀÛ¾÷À» ÇÏ´Â »ç¶÷µé ƯÈ÷ °Ç¹Ý ¾Ç±â¸¦ ¿¬ÁÖ°¡, ŸÀÚ¼ö ±×¸®°í ÀÚ·á °ü¸®ÀÚ µî°ú °°Àº »ç¶÷¿¡°Ô Àå¾Ö°¡ ¹ß»ýÇÑ´Ù. 2. ¼ö±Ù°ü³» Á¤Áß ½Å°æÀÌ ¾Ð¹ÚµÉ ¶§ ÀϾ´Â ÁõÈıºÀ¸·Î¼­, ¼Õ°¡¶ôÀÇ µ¿Åë, ÀÛ¿­°¨ ±×¸®°í ÀÌ»ó °¨°¢À» µ¿¹ÝÇϸç, ¶§·Î´Â ÆÈ²ÞÄ¡±îÁö ÆÄ±ÞµÈ´Ù. 3. ¼ö±Ù°üÀº ¼Õ¸ñÀÇ ¼öÀåºÎ¿¡ À§Ä¡Çϸç, ¹èÃø°ú Ãøº®Àº ¼ö±Ù°ñ·Î ±¸¼ºµÇ°í, º¹ÃøÀº ´Ü´ÜÇÑ ¼¶À¯¼º Ⱦ¼ö±Ù Àδë·Î µ¤Çô ÅͳÎÀ» Çü¼ºÇÑ´Ù. Åͳγ»¿¡´Â Á¤Áß ½Å°æ, õÁö±¼±Ù, ½ÉÁö±¼±Ù, À幫Áö±¼±ÙÀÌ Åë°úÇϴµ¥ Á¤Áß ½Å°æÀÇ ¾Ð¹ÚÀ¸·Î ¹ß»ýÇÏ´Â ÁõÈıºÀÌ´Ù.
  • Carpenter syndrome
    Ä«¾ÆÆæÅÍ ÁõÈıº
    ÷µÎ, ´ÙÁö ÇÕÁöÁõ, ´ÜÁöÁõ, ÀÌ»ó ¾È¸é, ºñ¸¸Áõ, Áö´ÉÀúÇÏ, ¼º¼± ±â´É ºÎÀüÀ» µ¿¹ÝÇÏ´Â »ó¿°»öü ¿­¼º À¯Àü¼º ÁõÈıº.
  • cartoid sinus syndrome
    °æµ¿¸Æµ¿ ÁõÈıº
  • catcry syndrome
    ¹¦¼º ÁõÈıº
  • cauda equina syndrome
    ¸¶¹Ì ÁõÈıº
  • cell-mediated immunodeficiency syndrome
    ¼¼Æ÷¼º ¸é¿ª °áÇÌ ÁõÈıº
  • cerebrohepatorenal syndrome
    ³ú°£ ½Å ÁõÈıº
  • cervical fusion syndrome
    °æºÎ À¯ÇÕ ÁõÈıº
  • cervicobrachial syndrome
    °æ »ó¿Ï ÁõÈıº
  • Cestans syndrome
    ¼¼½ºÅº ÁõÈıº
  • Charcot-Wilbrand syndrome
    »þ¸£ÄÚ-ºôºê¶õµå ÁõÈıº
  • chiasmal syndrome
    ½Ã ½Å°æ ±³Â÷ºÎ ÁõÈıº
  • Chilaiditis syndrome
    ų¶óÀÌµðÆ¼ ÁõÈıº
    °áÀå ¶Ç´Â ¼ÒÀåÀÇ ÀϺΰ¡ °£°ú Ⱦ°æ¸· »çÀÌ¿¡ °¨µ·ÇÏ¿© ÀϾ´Â ÁõÈıº.
  • cholecysto-hepatic flexure adhesion syndrome
    ´ã³¶ °áÀå °£°îºÎ À¯Âø ÁõÈıº
  • Chotzen's syndrome
    ÄÚþ ÁõÈıº
    ÷µÎÇÕÁöÁõÀ» ³ªÅ¸³»´Â »ó¿°»öü¼º ¿ì¼ºÀ¸·Î À¯ÀüµÇ´Â À¯Àü¼º Áúȯ.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 12
Bartter's syndrome <syndrome> A clinical syndrome characterised by enlargement of certain kidney cells, alkalosis, hypokalaemia and increased production of the hormone aldosterone. Common in children and may be seen in dwarfism.
(27 Sep 1997)
basal cell nevus syndrome <syndrome> An inherited group of defects which involve abnormalities of the skin, eyes, nervous system, endocrine, glands and bones.
The condition is characterised by an unusual facial appearance and a predisposition for skin cancer.
(27 Sep 1997)
Basan's syndrome <syndrome> Ectodermal dysplasia with hypotrichosis, hypohidrosis, defective teeth, and unusual dermatoglyphics.
(05 Mar 2000)
Bassen-Kornzweig syndrome <syndrome> A rare congenital disorder that causes the body to not produce chylomicrons, low density lipoprotein (LDL) and very low density lipoprotein (VLDL). Individuals with this condition are unable to properly digest fats. Other findings include ataxia, peripheral neuropathy and other forms of nerve dysfunction.
Treatment includes vitamin E.
(27 Sep 1997)
battered child syndrome <radiology> Multiple assymetrical fractures, separation of distal epiphyses, irregularity and fragmentation of metaphyses, bucket-handle fracture, corner fracture of elbow, knee, ankle (sudden twisting motion), isolated spiral fracture, extensive periosteal reaction (subperiosteal haemorrhage), exuberant callus formation, cortical hyperostosis extending to epiphyseal plate, avulsion fracture at ligamentous insertion, subdural haematoma (most common), brain atrophy (up to 100%), infarction (50%), subdural hygroma, encephalomalacia, porencephaly
(12 Dec 1998)
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)
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