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"elfin facies 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®
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  • 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¿À¸®ÇÉÁõÈıº
  • anticardiolipin syndrome
    Ç×Ä«¸£µð¿Ã¸®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)
  • aortitis syndrome
    ´ëµ¿¸Æ¿°ÁõÈıº(¡­æúñøý¦ÏØ).
  • aortitis syndrome
    ´ëµ¿¸Æ¿° ÁõÈıº(¡­ñøý¦ÏØ)
  • apallic syndrome
    ¹«½ÉÁõÈıº(Ùíãýñøý¦ÏØ)
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  • dermatorheumatismal syndrome
    ÇǺηù¸¶Æ¼½ºÁõÈıº(¡­ñøý¦ÏØ).
  • diencephalic syndrome
    °£³úÁõÈıº(ÊàÒàñøý¦ÏØ).
  • digeorge syndrome
    DiGeorge ÁõÈıº(¡­ñøý¦ÏØ), µðÁÒ¿ÀÁö ÁõÈıº
  • disappearing bile duct syndrome
    ´ãµµ¼Ò½ÇÁõÈıº
  • discontinuation syndrome
    ºÒ¿¬¼Ó¼º ÁõÈıº
  • discrete multiple endocrine adenomatosis syndrome
    ºÐ¸®¼º ´Ù¹ß ³»ºÐºñ¼±Á¾ ÁõÈıº(ÝÂìÆàõÒýÛ¡Ò®ÝÂù²àÍðþñøý¦ÏØ).
  • dissacharidase deficiency syndrome
    ÀÌ´ç·ùºÐÇØÈ¿¼Ò °áÇÌÁõÈıº(¡­ÌÀù¹ñøý¦ÏØ ).
  • dorsal midbrain syndrome
    ÈÄÁß³úÁõÈıº
  • double crush syndrome
    ÀÌÁß ºÐ¼â ÁõÈıº
  • down syndrome
    ´Ù¿îÁõÈıº(¡­ñøý¦ÏØ)
  • downs syndrome
    ´Ù¿îÁõÈıº
  • dresslers syndrome
    dresslerÁõÈıº
  • dresslers syndrome
    µå·¹½½·¯ ÁõÈıº(¡­ñøý¦ÏØ)
  • dry eye syndrome
    °Ç¼º¾ÈÁõÈıº
  • duane retraction syndrome
    µÎ¿£±Û ÀÌ»óÁõÈıº
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ARC accelerating rate calorimetry; acquired immunodeficiency syndrome-related complex; active renin conc...
ARDS acute respiratory distress syndrome; adult respiratory distress syndrome
AWS Alagille-Watson syndrome; alcohol withdrawal syndrome
BCS battered child syndrome; blood cell separator; British Cardiac Society; Budd-Chiari syndrome
BIS bone cement implantation syndrome; Brain Information Service; building illness syndrome
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GSS Gerstmann-Straussler-Scheinker Syndrome
GSS Gerstmann-Strausler syndrome
GS Gilbert Syndrome
GTS Gilles de la Tourette Syndrome
GPS Gray platelet syndrome
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  • 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
  • hypokinetic syndrome
    °ú¼Ò¿îµ¿¼º Áõ¼¼, ¿îµ¿ ÀúÇÏ ÁõÈıº, ¿îµ¿ ÀúÇϼº ÁõÈıº, °ú¼Ò¿îµ¿¼º ÁõÈıº
  • hypomelia-hypotrichosis-facial haemangioma syndrome
    ´ÜÁö-ºó¸ð-¾È¸é Ç÷°üÁ¾ ÁõÈıº
  • hypoplastic right heart syndrome
    ¿ì½É½Ç Çü¼º ºÎÀü ÁõÈıº
  • hypotonic syndrome
    ÀúÀå ÁõÈıº
  • hypoventilation syndrome
    È£Èí ÀúÇÏ ÁõÈıº
  • ICE syndrome
    ȫä °¢¸· ³»ÇÇ ÁõÈıº
    iridocorneal endothelial syndromeÀÇ ¾àÀÚ.
  • ileal diverticulum meckel syndrome
    µ¹ âÀÚ °ç ÁÖ¸Ó´Ï ¸ßÄÌ ÁõÈıº
  • immersion foot syndrome
    ħ¼öÁ· ÁõÈıº
  • immune amnesia syndrome
    ¸é¿ª ±â¾ï »ó½Ç ÁõÈıº
  • immunoproliferative syndrome
    ¸é¿ª Áõ½Ä¼º ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 20
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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