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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®
    ÇѱÛ
  • 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
  • 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).
  • anorectal syndrome
    Ç×¹®Á÷ÀåÁõÈıº(ùýÚ¦òÁ ñøý¦ÏØ).
  • anorectal syndrome
    Ç×¹®Á÷ÀåÁõÈıº(Ç×¹®Á÷ÀåÁõÈıº).
  • anterior chamber cleavage syndrome
    Àü¹æ(°¢)ºÐ¸®ºÎÀüÁõÈıº
  • anterior choroidal artery occlusion syndrome
    Àü¸Æ¶ôÃѵ¿¸Æ Æó¼âÁõÈıº.
  • anterior cornual syndrome
    Àü°¢ÁõÈıº(îñÊÇñøý¦ÏØ).
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  • ¿µ¹®
    ÇѱÛ
  • culture-bound syndrome
    ¹®È­±Ç ÁõÈıº(ÙþûùÏêñøý¦ÏØ)
  • cystic duct syndrome
    ´ã³¶°üÁõÈıº(¡­ñøý¦ÏØ).
  • cystic duct syndrome
    ´ã³¶°üÁõÈıº(¡­ÁõÈıº).
  • dandy-walker syndrome
    ´íµð¿öÄ¿ ÁõÈıº (¡­ñøý¦ÏØ)
  • de Clerambault syndrome
    ²ô·¹¶ûº¸¿À ÁõÈıº(~ñøý¦ÏØ)
  • de la Tourettes syndrome
    ¶Ñ·¿ÁõÈıº(~ñøý¦ÏØ)
  • de-toni-Debre-Fanconi syndrome
    µðÅä´Ïµðºê¸®ÆÇÄÚ´ÏÁõÈıº
  • defibrination syndrome
    Å»¼¶À¯¼Ò ÁõÈıº(÷­àéë«áÈñøý¦ÏØ)
  • deficient syndrome, antibody
    Ç×ü°áÇÌÁõÈıº
  • deficit syndrome
    °áÇÌÁõÈıº(ÌÀù¹ñøý¦ÏØ)
  • delayed sleep phase syndrome
    Áö¿¬¼º ¼ö¸é»ó ÁõÈıº(òÀæÅàõ â²ØùßÓ ñøý¦ÏØ)
  • denial- of- deficit syndrome
    °áÇÌ ºÎÁ¤ ÁõÈıº(ÌÀù¹ÜúïÒñøý¦ÏØ)
  • dento-oculo-cutaneous syndrome
    Ä¡¾Æ ´« ÇǺΠÁõÈıº
  • denys-drash syndrome
    Denys-DrashÁõÈıº(¡­ñøý¦ÏØ)
  • depersonalization-derealization syndrome
    ÀÌÀÎ-ºñÇö½Ç°¨ ÁõÈıº(ì¶ìÑ-ÞªúÞãùÊï ñøý¦ÏØ)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 19
Z-E Syndrome Zollinger-Ellison Syndrome
ACS acrocallosal syndrome; acrocephalosyndactyly; acute chest syndrome; acute confusional state; Alcon C...
ADFN albinism-deafness [syndrome]; albinism-deafness syndrome
AGS adrenogenital syndrome; Alagille syndrome; American Geriatrics Society; audiogenic seizures
AMS ablepharon-microstomia syndrome; acute mountain sickness; adenosylmethionine synthetase; aggravated ...
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FRA(X) Fragile X syndrome
FRAXA Fragile X syndrome
FXS Fragile X syndrome
GWS GABA Withdrawal Syndrome
GS Gardner Syndrome
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  • ¿µ¹®
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    ¼³¸í
  • 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.
  • Horton's syndrome
    Horton ÁõÈıº
    cluster headache¸¦ º¸½Ã¿À.
  • Hurler-Scheie syndrome
    Çæ·¯-»þÀÌ¿¡ ÁõÈıº
  • Hutchinson's syndrome
    ÇãÄ£½¼ ÁõÈıº
    °£Áú °¢¸·¿°, ¹Ì·Î Áúȯ, ÇãÄ£½¼ Ä¡¾ÆÀÇ º¹ÇÕÀ¸·Î ¼±Ãµ ¸Åµ¶¿¡¼­ º¼ ¼ö ÀÖ´Ù. ¼±Ãµ¼º ¸Åµ¶ÀÇ Áõ»óÀ¸·Î ÇãÄ£½¼ 3ÁÖÁõÀ¸·Î Áø´ÜÇÒ ¼ö ÀÖ´Ù. ¸Åµ¶Àº 1Â÷, 2Â÷, 3Â÷ÀÇ ´Ü°è¸¦ º¸À̸ç À¯Àü¼ºÀ» ¶ì°í ÀÖ´Ù.
  • hyperimmunoglobulin E syndrome
    °ú¸é¿ª ±Û·ÎºÒ¸° E ÁõÈıº
  • hyperkinetic heart syndrome
    °ú¿îµ¿¼º ½ÉÁõÈÄ, °ú¿îµ¿¼º ½ÉÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 19
A-V strabismus syndrome <syndrome> Strabismus in which the angle of deviation is more marked on looking upward or downward.
See: A-esotropia, V-esotropia, A-exotropia, V-exotropia.
(05 Mar 2000)
Ayerza's syndrome <syndrome> Sclerosis of the pulmonary arteries in chronic cor pulmonale; associated with severe cyanosis, it is a condition resembling polycythemia vera but resulting from primary pulmonary arteriosclerosis or primary pulmonary hypertension and characterised by plexiform lesions of arterioles.
Synonym: Ayerza's disease, cardiopathia nigra, plexogenic pulmonary arteriopathy.
(05 Mar 2000)
Babinski's syndrome <syndrome> The combination of cardiac, arterial, and central nervous system manifestations of late syphilis.
(05 Mar 2000)
baby bottle syndrome Rampant caries of the primary dentition associated with the habitual use, after age 1, of a baby bottle as an aid for sleeping.
Synonym: baby bottle syndrome.
(05 Mar 2000)
baby, foetal alcohol syndrome <syndrome> Alcohol is capable of causing birth defects. FAS (foetal alcohol syndrome) always involves brain damage. And impaired growth. FAS also always involves head and face abnormalities. No amount of alcohol has been proven safe during pregnancy. Women who are or may become pregnant are advised to avoid alcohol.
(12 Dec 1998)
Balint's syndrome <syndrome> An entity characterised by optic ataxia and simultanagnosia. This difficulty in applying the visual system to a visual task is usually due to damage to the superior temporal-occipital areas in both hemispheres.
(05 Mar 2000)
Bamberger-Marie syndrome hypertrophic pulmonary osteoarthropathy
Bannwarth's syndrome <syndrome> Neurologic manifestations of Lyme disease, also called chronic lymphocytic meningitis and tick-borne meningopolyneuritis.
(05 Mar 2000)
Banti's syndrome <syndrome> Chronic congestive splenomegaly that occurs primarily in children as a sequel to hypertension in the portal or splenic veins, usually as a result of thrombosis of the veins; anaemia, splenomegaly, and irregular episodes of gastrointestinal bleeding are usually observed, with ascites, jaundice, leukopenia, and thrombocytopenia developing in various conbinations.
Synonym: Banti's disease, splenic anaemia.
(05 Mar 2000)
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)
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