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  • ¿µ¹®
    ÇѱÛ
  • exfoliation syndrome
    ¹ÚÅ»ÁõÈıº
  • ectrodactyly-ectodermal dysplasia clefting syndrome
    °áÁö¿Ü¹è¿±Çü¼ºÀ̻󰥸²ÁõÈıº
  • extrapyramidal syndrome
    ÇǶó¹Ìµå¹Ù±ù±æÁõÈıº, Ãßü¿Ü·ÎÁõÈıº
  • empty nest syndrome
    ºóµÕÁöÁõÈıº
  • empty sella syndrome
    ºó¾ÈÀåÁõÈıº
  • entrapment syndrome
    Æ÷ÂøÁõÈıº
  • eosinophilia-myalgia syndrome
    È£»ê±¸Áõ°¡±Ù(À°)ÅëÁõÁõÈıº
  • epidermal nevus syndrome
    Ç¥ÇǸð¹ÝÁõÈıº
  • ectopic ACTH syndrome
    µý°÷ºÎ½Å°ÑÁúÀÚ±ØÈ£¸£¸óÁõÈıº, À̼ҼººÎ½ÅÇÇÁúÀÚ±ØÈ£¸£¸óÁõÈıº
  • facet syndrome
    ÈİüÀýÁõÈıº
  • Felty¡¯s syndrome
    ÆçƼÁõÈıº
  • fertile eunuch syndrome
    °¡ÀÓ°íÀÚÁõÈıº
  • fetal alcohol syndrome
    žƾËÄÚ¿ÃÁõÈıº
  • fetal distress syndrome
    žưï¶õÁõÈıº
  • fetal hydantoin syndrome
    žÆÈ÷´ÜÅäÀÎÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
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  • cranial nerve syndrome
    ³ú½Å°æÁõÈıº
  • craniofacial syndrome
    ¸Ó¸®¾ó±¼ÁõÈıº
  • cri du chat syndrome
    (¢¡cat¡¯s cry) °í¾çÀÌ¿ïÀ½ÁõÈıº
  • cubital tunnel syndrome
    ÆÈ²ß±¼ÁõÈıº
  • culture-bound syndrome
    ¹®È­±ÇÁõÈıº
  • defibrination syndrome
    Å»¼¶À¯¼ÒÁõÈıº
  • deficit syndrome
    °áÇÌÁõÈıº
  • depersonalization-derealization syndrome
    ÀÌÀκñÇö½Ç°¨ÁõÈıº
  • discontinuation syndrome
    ºÒ¿¬¼ÓÁõÈıº
  • dissociation syndrome
    ÇØ¸®ÁõÈıº
  • dry eye syndrome
    ´«¸¶¸§ÁõÈıº, ¸¶¸¥´«ÁõÈıº
  • dumping syndrome
    ´ýÇÎÁõÈıº
  • dyskinetic syndrome
    ÀÌ»ó¿îµ¿ÁõÈıº
  • electrolyte deficiency syndrome
    ÀüÇØÁú°áÇÌÁõÈıº
  • empty nest syndrome
    ºóµÕÁöÁõÈıº
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  • Hamman Rich syndrome =diffuse interstitial pulmonary fibrosis
    ÇØ¸Õ- ¸®Ä¡ÁõÈıº.
  • Hamman-Rich syndrome
    ÇØ¸Õ-¸®Ä¡ ÁõÈıº
  • Heerfordts syndrome => uveoparotid fever
    Ç츣Æ÷¸£Æ® ÁõÈıº
  • Henoch Schoenlein syndrome
    Çì³ëÈ£-½¨¶óÀÎÁõÈıº.
  • Henoch Schoenlein syndrome
    Çì³ëÈ£-½¨¶óÀÎÁõÈıº
  • Hermansky-Pudlak syndrome
    Ç츣¸¸½ºÅ°-Ǫµé¶óÅ© ÁõÈıº
  • Hermansky-Pudlak syndrome => oculocutaneous albinism
    ¾È±¸ ÇǺΠ¹é»öÁõ
  • Hoffmann s syndrome
    È£ÇÁ¸¸ÁõÈıº.
  • Holt Oram syndrome
    ȦƮ-¿À¶÷ÁõÈıº.
  • Horners syndrome
    È£³Ê ÁõÈıº
  • Horners syndrome
    È£³Ê¾¾ ÁõÈıº
  • Horners syndrome
    È£¸£³ÊÁõÈıº
  • Hunters syndrome => mucopolysaccharidosis
    ÇåÅÍ ÁõÈıº
  • Hurler syndrome
    Èĸ¦·¯ÁõÈıº
  • Hurlers syndrome => mucopolysaccharidosis
    Èĸ¦·¯ ÁõÈıº
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  • aids=£¾acquired immune deficiency syndrome
    ÈÄõ¼º¸é¿ª°áÇÌÁõÈıº(ý­ô¸àõØóæ¹ÌÀù¹ñøý¦ÏØ)
  • albrights syndrome
    ¾ËºÎ¶óÀÌÆ® ÁõÈıº(¡­ñøý¦ÏØ)
  • alports syndrome
    ¾ËÆ÷¿ÀÆ®ÁõÈıº
  • alports syndrome(disease)
    ¾ËÆ÷Æ® ÁõÈıº(º´)(¡­ñøý¦ÏØ)
  • alveolar hypoventilation syndrome
    ÆóÆ÷Àúȯ±âÁõÈıº.
  • alveolar-capillary block syndrome
    ÆóÆ÷-¸ð¼¼Ç÷°üÂ÷´ÜÁõÈıº.
  • amelo-cerebro-hypohidrotic syndrome
    ¿¡³ª¸á-´ë³ú-¶¡°ú¼ÒÁõÈıº
  • amnestic syndrome
    °Ç¸ÁÁõÈıº(¡­ñøý¦ÏØ).
  • amniotic band syndrome
    ¾ç¸·´ëÁõÈıº(¡­Óáñøý¦ÏØ)
  • androgen insensitivity syndrome
    ¾Èµå·Î°Õ( ³²¼ºÈ£¸£¸ó) ºÒ°¨¼º ÁõÈıº(ÝÕÊïàõ ñøý¦ÏØ)
  • androgen-resistance syndrome
    ³²¼ºÈ£¸£¸ó ³»¼º(ÀúÇ×)ÁõÈıº?
  • anginal syndrome
    Çù½ÉÁõÁõÈıº (¡­ñøñøý¦ÏØ).
  • angioosteohypertrophy syndrome
    Ç÷°ü °ñºñÈÄ ÁõÈıº(úìη ÍéÝþý§ ñøý¦ÏØ)
  • anorectal syndrome
    Ç×¹®Á÷ÀåÁõÈıº(ùýÚ¦òÁ ñøý¦ÏØ).
  • anorectal syndrome
    Ç×¹®Á÷ÀåÁõÈıº(Ç×¹®Á÷ÀåÁõÈıº).
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SSS scalded skin syndrome; secondary Sjogren syndrome; sick sinus syndrome; specific soluble substance; ...
ASDC Association of Sleep Disorders Centers; ¹Ì±¹ ¼ö¸é Áúȯ ¼¾ÅÍ Çùȸ
CSA   1) Cell Surface Antigen
  2) Central Sleep Apnea
DIMS Disorders of Initiating & Maintaining Sleep; ÀÔ¸éÀå¾Ö ¹× ¼ö¸é À¯Áö Àå¾Ö; ºÒ¸éÁõ
DSIP Delta Sleep Inducing Peptide
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TST Total Sleep Time
DS desynchronized sleep
NREM non-rapid eye movement sleep
S2 sleep
SOREMP sleep onset rapid eye movement period
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    ¼³¸í
  • clumsy hand syndrome
    ¼­Å÷ ¼Õ ÁõÈıº
  • co-contraction syndrome
    µ¿½Ã ¼öÃà ÁõÈıº
  • Cockayne syndrome
    ÄÚÄÉÀÎ ÁõÈıº
  • Coffin-Lowry syndrome
    ÄÚÇÉ-·Î¸® ÁõÈıº
  • Cogan-Reese syndrome
    ÄÚ°£-¸®½º ÁõÈıº
  • congenital fibrosis syndrome
    ¼±Ãµ ¼¶À¯Áõ ÁõÈıº
  • congenital Q-T syndrome
    ¼±Ãµ¼º QT ÁõÈıº
  • congenital rubella syndrome
    ¼±Ãµ¼º dzÁø ÁõÈıº
    žư¡ ¸ðü ³»¿¡¼­ dzÁø ¹ÙÀÌ·¯½º¿¡ Ä§ÇØµÇ¾î »ý±â´Â ÀÌ»ó Áõ¼¼. ÀӽŠÃʱâÀÇ ÀÓ»êºÎ°¡ dzÁø¿¡ °É¸®¸é žư¡ ¹ßÀ° Ãʱ⿡ dzÁø ¹ÙÀÌ·¯½º¿¡ Ä§ÇØµÇ¾î Ãâ»ý ÈÄ¿¡ ´«ÀÇ ÀÌ»ó
  • conjunctivo-urethro-synovial syndrome
    °á¸· ´¢µµ Ȱ¸· ÁõÈıº
  • Conn syndrome
    ÄÜ ÁõÈıº
  • contiguous gene syndrome
    Á¢Ã˼º À¯ÀüÀÚ ÁõÈıº
  • cord compression syndrome
    ô¼ö ¾Ð¹Ú ÁõÈıº
  • corpus callosum syndrome
    ³ú·® ÁõÈıº
  • Cowden syndrome
    ÄÚ¿ìÅÙ ÁõÈıº
    ½Å»ý¹° ÁõÈıº. À¯µÎÁ¾°ú ºñ½ÁÇÑ º´¼Ò·Î ÀÚ°¥°°Àº ÇüÅÂÀÎ ¼¶µàÁ¾ÀÌ´Ù.
  • cracked tooth syndrome
    ±Õ¿­Ä¡ Áõ»ó, ±Õ¿­Ä¡ ÁõÈıº, ÆÄÀýÄ¡ ÁõÈıº
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Bardet-Biedl syndrome <syndrome> Mental retardation, pigmentary retinopathy, polydactyly, obesity, and hypogenitalism; recessive inheritance.
See: Laurence-Moon-Biedl syndrome.
(05 Mar 2000)
bare lymphocyte syndrome <syndrome> Absence of HLA antigens on peripheral mononuclear cells, which may result in immunodeficiency.
(05 Mar 2000)
Barlow's syndrome <syndrome> Also referred to as mitral valve prolapse, systolic click-murmur syndrome, floppy-valve syndrome and billowing mitral leaflet syndrome. A common, but highly variable (most individuals are asymptomatic), clinical syndrome that has been described in up to 7% of all females in the 14 to 30 age group. There is also an increased familial incidence suggesting an autosomal dominant form of inheritance.
(27 Sep 1997)
Barlow syndrome <syndrome> Late apical systolic murmur or (so-called "mid-late") systolic click, or both, due to massive billowing of the anterior and/or posterior (mural) mitral valvular leaflet into the left atrial cavity (also, floppy valve syndrome); electrocardiographically, ST-T changes in a posteroinferior distribution resembling those of myocardial ischemia often coexist for unknown reasons; rhythm disturbances may coexist with this syndrome without demonstrable pathogenetic relationship.
(05 Mar 2000)
Barrett's syndrome <syndrome> Chronic peptic ulceration of the lower oesophagus, which is lined by columnar epithelium, resembling the mucosa of the gastric cardia, acquired as a result of long-standing chronic oesophagitis; oesophageal stricture with reflux, and adenocarcinoma, also have been reported.
Synonym: Barrett's oesophagus.
(05 Mar 2000)
Bart's syndrome <syndrome> A form of epidermolysis bullosa with blistering of the extremities and intertriginous areas, erosions of the mouth, and deformed nails; probably autosomal dominant; there is often spontaneous improvement with no residual scarring.
(05 Mar 2000)
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)
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