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"immunologic deficiency 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
  • Turners syndrome
    ÅÍ³Ê ÁõÈıº
  • Ushers syndrome
    ¾Æ¼ÅÁõÈıº
  • V-syndrome
    VÁõÈıº
  • V-syndrome
    V ÁõÈıº
  • Vogt-Koyanagi syndrome
    Æ÷±×Æ® °í¾ß³ª±â ÁõÈıº
  • Vogt-Koyanagi-Harada syndrome
    º¸Å©Æ®-°í¾ß³ª±â-Ç϶ó´Ù ÁõÈıº
  • WPW syndrome
    WPWÁõÈıº, ºÎÀüµµ·ÎÁõÈıº .
  • Waardenburgs syndrome
    ¹Ù¸£µ§ºÎ¸£Å© ÁõÈıº
  • Wallenbergs syndrome
    ¹ß·»º£¸£Å©ÁõÈıº.
  • Waterhouse Friderichsen syndrome
    ¿ö¾îÅÍÇϿ콺-ÇÁ¸®µ¥¸®Å©¼¾ÁõÈıº.
  • Waterhouse-Friderichsen syndrome
    ¿öÅÍÇϿ콺-ÇÁ¸®µ¥¸¯¼¾ ÁõÈıº
  • Weber syndrome
    ¿þ¹öÁõÈıº
  • Weber-Cocayne syndrome
    ¿þ¹ö ÄÚÄÉÀÎ ÁõÈıº
  • Webers syndrome
    ¿þ¹öÁõÈıº.
  • Werners syndrome
    º£¸£³ÊÁõÈıº.
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  • ¿µ¹®
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  • atypical schizophrenic syndrome
    ºñÁ¤Çü Á¤½ÅºÐ¿­¼º ÁõÈıº
  • auriculotemporal nerve syndrome
    À̰³ÃøµÎ½Å°æÁõÈıº.
  • auriculotemporal syndrome
    À̰³ÃøµÎÁõÈıº(¡­ñøý¦ÏØ).
  • auriculotemporal syndrome
    À̰³ÃøµÎ ÁõÈıº(ì¼Ë¿ö°Ôé ñøý¦ÏØ)
  • bantis syndrome
    ¹ÝƼÁõÈıº(¡­ñøý¦ÏØ)
  • bartters syndrome
    ¹ÙÅÍ ÁõÈıº(¡­ñøý¦ÏØ)
  • basal cell nevus syndrome
    ±âÀú¼¼Æ÷¸ð¹ÝÁõÈıº(¡­Ù½Úèñøý¦ÏØ).
  • basal cell nevus syndrome
    ±âÀú¼¼Æ÷¸ð¹ÝÁõÈıº(¡­Ù½Úèñøý¦ÏØ)
  • basilar syndrome
    ³úÀúµ¿¸ÆÁõÈıº(¡­ÔÑØæñøý¦ÏØ).
  • battered child syndrome
    ¸Å¸Â´Â¾Æµ¿ ÁõÈıº
  • battered child syndrome
    ¸Å¸Â´Â¾ÆÀÌÁõÈıº
  • beckwith-wiedemann syndrome
    º£Å©À§µå-À§µå¸¸ ÁõÈıº(¡­ñøý¦ÏØ)
  • bernard-soulier syndrome
    ¹ö³ªµå-½¶¸®¾î ÁõÈıº(¡­ñøý¦ÏØ)
  • big heart syndrome
    °Å½ÉÁõÈıº(ËÝãýñøý¦ÏØ)
  • big heart syndrome
    °Å½ÉÁõÈıº(ËÝãýñøý¦ÏØ).
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OTCD ornithine carbomoyltransferase deficiency
PFFD proximal focal femoral deficiency
QD Qi deficiency
QYD Qi and Yin deficiency
SAPD sphingolipid activator protein deficiency
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CRPS-I Complex Regional Pain Syndrome Type I
CNS Congenital Nephrotic Syndrome
CRS Congenital Rubella Syndrome
CCHS Congenital central hypoventilation syndrome
CS Cowden syndrome
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  • Libman Sachs syndrome
    ¸®ºê¸¸-ÀÛ½º ÁõÈıº
  • linear nevus sebaceous syndrome
    ¼±»ó ¸ð¹Ý ÇÇÁö¼± ÁõÈıº
  • lobotomy syndrome
    ³ú¿± Àý´Ü¼ú ÁõÈıº
  • lock pin ¼±´ÜÀº taperÇÏ°í µÎºÎ´Â ±¸»óÀ¸·Î µÇ¾î ÀÖ´Â Ä¡³»°ñ³» ¸Å½ÄüÀÇ ÀÏÁ¾.

    locked-in syndrome

    Æó¼â ÁõÈıº
  • long tract syndrome
    Àå°æ·Î ÁõÈıº
  • low output syndrome
    Àú ¹ÚÃâ·® ÁõÈıº
  • low salt syndrome
    Àú¿° ÁõÈıº
  • lower nephron syndrome
    ÇϺΠ³×ÇÁ·Ð ÁõÈıº
  • lupus erythematosus like syndrome
    È«¹Ý¼º ·çǪ½º¾ç ÁõÈıº
  • lupus-like syndrome
    ³¶Ã¢ ¾ç»óÀÇ ÁõÈıº
  • luxury perfusion syndrome
    ȣȭ °ü·ù ÁõÈıº
  • Lyell syndrome
    Lyell ÁõÈıº
  • malabsorption syndrome
    Èí¼öÀå¾Ö ÁõÈıº
    Á¤°ü¿¡¼­ÀÇ ¿µ¾ç¹° Èí¼öÀÇ Àå¾Ö¸¦ °¡Á®¿À´Â ÁúȯÀ» ÃѰýÇÏ´Â ¸íĪ. ¼³»ç, üÁß °¨¼Ò, ¿µ¾ç½ÇÁ¶¸¦ °¡Á®¿À´Â ¿øÀÎÀÌ µÇ´Â ÁúȯÀº Àå°ü ¼ö¼ú µÚ, Àå Áúȯ, ÃéÀå Áúȯ, °£´ãµµ Áúȯ, ¸²ÇÁÁ¾, ½ÉºÎÀü, ½É³¶¿°, ¾Æ´Ò·ÎÀ̵å½Ã½º, ¥â-Áö¹æ ´Ü¹é °á¼ÕÁõ, ½ºÇª·ç¿ì
  • maladaptation syndrome
    ÀûÀÀ Àå¾Ö ÁõÈıº
  • male Turners syndrome
    ³²¼º ÅÍ³Ê ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 20
Briquet's syndrome <syndrome> A chronic but fluctuating mental disorder, usually of young women, characterised by frequent complaints of physical illness involving multiple organ systems simultaneously.
(05 Mar 2000)
Brissaud-Marie syndrome <syndrome> Unilateral spasm of the tongue and lips, of hysterical nature.
(05 Mar 2000)
Brock's syndrome Atelectasis of the right middle pulmonary lobe, with chronic pneumonitis.
(12 Dec 1998)
Brown-Sequard's syndrome <neurology, syndrome> A type of spinal cord lesion that is characterised by hemiparaplegia and hyperesthesia, but with loss of motor function on the same side as the lesion and hemianaesthesia on the opposite side.
(27 Sep 1997)
brown-sequard syndrome <syndrome> A syndrome due to damage of one half of the spinal cord, resulting in ipsilateral paralysis below the level of the lesion and loss of discriminatory and joint sensation, and contralateral loss of pain and temperature sensation. Brown-sequard was a french physiologist, 1817-1894. The syndrome is also called brown-sequard disease and brown-sequard paralysis but this latter should not be confused with a flaccid paralysis seen in disorders of the urinary tract called by the same name.
(12 Dec 1998)
brown's syndrome <syndrome> An ophthalmology (eye) problem. Brown's syndrome presents as an abnormality at birth (congenitally) and is characterised by an inability to elevate the eyeball when also trying to move the eyeball to the outside. Brown's syndrome can also occur because of other conditions which affect the normal function of the eye muscles.
(12 Dec 1998)
Brugsch's syndrome <radiology> Idiopathic, familial hypertrophic osteoarthropathy, boys at puberty, blacks more than whites, familial, periosteal reaction, thick skin: extremities and forehead, hyperhidrosis, relatively pain free
(12 Dec 1998)
Budd-Chiari syndrome <gastroenterology, syndrome> Liver dysfunction due to occlusion of the hepatic veins. May be congenital.
(27 Sep 1997)
Budd's syndrome <syndrome> Thrombosis of the hepatic vein with great enlargement of the liver and extensive development of collateral vessels, intractable ascites, and severe portal hypertension.
Synonym: Budd's syndrome, Budd-Chiari syndrome, Chiari's disease, Chiari-Budd syndrome, Rokitansky's disease.
(05 Mar 2000)
Burger-Grutz syndrome Hyperlipoproteinaemia characterised by the presence of large amounts of chylomicrons and triglycerides in the plasma when the patient has a normal diet, and their disappearance on a fat-free diet; low alpha-and beta-lipoproteins on a normal diet, with increase on fat-free diet; decreased plasma postheparin lipolytic activity; and low tissue lipoprotein lipase activity. It is accompanied by bouts of abdominal pain, hepatosplenomegaly, pancreatitis, and eruptive xanthomas; autosomal recessive inheritance.
See: familial lipoprotein lipase inhibitor.
Synonym: Burger-Grutz syndrome, familial fat-induced hyperlipaemia, familial hyperchylomicronaemia, familial hypertriglyceridemia, idiopathic hyperlipaemia.
(05 Mar 2000)
burner syndrome <syndrome> Multiple episodes of upper extremity burning pain, sometimes accompanied by shoulder girdle weakness, experienced during contact sports, especially football, with each forceful blow to the head or shoulder; attributed to an upper trunk brachial plexopathy.
(05 Mar 2000)
Burnett's syndrome <syndrome> A form of metabolic acidosis that can result from the excessive consumption of milk (calcium) and antacids (sodium bicarbonate) over a prolonged period of time. This can result in calcium deposits in the kidneys and body tissues.
Symptoms include nausea, vomiting and weakness. May be seen as a complication of peptic ulcer therapy.
(27 Sep 1997)
burning foot syndrome <syndrome> A disorder observed in prisoners-of-war in World War II, now believed to be due to a pantothenate deficiency.
(05 Mar 2000)
burning mouth syndrome <syndrome> A group of painful oral symptoms associated with a burning or similar sensation. There is usually a significant organic component with a degree of functional overlay; it is not limited to the psychophysiologic group of disorders.
(12 Dec 1998)
burning vulva syndrome <syndrome> Persistent vulvodynia in which a physical cause has not been identified.
(05 Mar 2000)
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