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"orbital floor 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
  • Cushing¡¯s syndrome
    Äí½ÌÁõÈıº
  • carotid sinus syndrome
    ¸ñµ¿¸Æ±¼ÁõÈıº, °æµ¿¸Æµ¿ÁõÈıº
  • carpal tunnel syndrome
    ¼Õ¸ñ±¼ÁõÈıº, ¼ö±Ù°üÁõÈıº
  • cast syndrome
    ¼®°íºØ´ëÁõÈıº
  • cat¡¯s cry syndrome
    °í¾çÀÌ¿ïÀ½ÁõÈıº
  • cat-eye syndrome
    °í¾çÀÌ´«ÁõÈıº
  • cauda equina syndrome
    ¸»ÃÑÁõÈıº, ¸¶¹ÌÁõÈıº
  • central cord syndrome
    Áß½Éô¼öÁõÈıº
  • central pain syndrome
    ÁßÃßÅëÁõÁõÈıº
  • Chinese restaurant syndrome
    Áß±¹À½½ÄÁõÈıº
  • camptomelic syndrome
    ±¼ÁöÁõÈıº
  • chromosomal breakage syndrome
    ¿°»öüÆÄ¼ÕÁõÈıº
  • chronic fatigue syndrome
    ¸¸¼ºÇÇ·ÎÁõÈıº
  • chronic pain syndrome
    ¸¸¼ºÅëÁõÁõÈıº
  • dry eye syndrome
    °Ç¼º¾ÈÁõÈıº, ¾È±¸°ÇÁ¶Áõ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
  • ¿µ¹®
    ÇѱÛ
  • chronic fatigue syndrome
    ¸¸¼ºÇÇ·ÎÁõÈıº
  • chronic pain syndrome
    ¸¸¼ºÅëÁõÁõÈıº
  • clinical syndrome
    ÀÓ»óÁõÈıº
  • clumsy child syndrome
    µÐÇѾƵ¿ÁõÈıº
  • clumsy hand syndrome
    ¼­Å÷¼ÕÁõÈıº
  • co-contraction syndrome
    µ¿½Ã¼öÃàÁõÈıº
  • combined immunodeficiency syndrome
    º¹Çո鿪°áÇÌÁõÈıº
  • compartment syndrome
    ±¸È¹ÁõÈıº
  • complex regional pain syndrome
    º¹ÇÕ±¹¼Òµ¿ÅëÁõÈıº
  • compression syndrome
    ¾Ð¹ÚÁõÈıº
  • concentration camp syndrome
    ¼ö¿ë¼ÒÁõÈıº
  • congenital constriction ring syndrome
    ¼±ÃµÇùÂø°í¸®ÁõÈıº
  • cor pulmonale syndrome
    Æó½ÉÀåÁõÈıº, ÇãÆÄ½ÉÀåÁõÈıº
  • cord compression syndrome
    ô¼ö¾Ð¹ÚÁõÈıº
  • cranial nerve syndrome
    ³ú½Å°æÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
  • ¿µ¹®
    ÇѱÛ
  • Feltys syndrome
    ÆçƼÁõÈıº
  • Forster-Kennedy syndrome
    Æ÷½ºÅÍ-Äɳ׵ð ÁõÈıº
  • Froin syndrome
    ÇÁ·Î¾ÞÁõÈıº
  • Gaisb cks syndrome
    °¡À̽ººÆÅ©ÁõÈıº
  • Ganser syndrome
    °µ¼­ÁõÈıº(~ñøý¦ÏÛ)
  • Ganser syndrome
    °µ¼­ÁõÈıº.
  • Gardner s syndrome
    °¡¾Æµå³ÊÁõÈıº.
  • Gianotti-Crosti syndrome => infantile papular acrodermatitis
    Àð³ëƼ Å©·Î½ºÆ¼ ÁõÈıº
  • Gilberts syndrome
    Áúº£¸£ÁõÈıº
  • Glucose-galactose malabsorption syndrome
    ±Û·çÄÚ¿À½º-°¥¶ôÅ佺Èí¼öÀå¾ÖÁõÈıº(ýåâ¥î¡äôñøý¦ÏØ)
  • Goldenhars syndrome->oculo-auriculo-vertebral dysplasia
    °ñµçÇÏÁõÈıº
  • Goltzs syndrome => focal dermal hypoplasia
    ±¹¼Ò ÁøÇÇ Çü¼ººÎÀüÁõ
  • Golzs syndrome
    °ñÁî ÁõÈıº
  • Goodpasture s syndrome
    ±¸µåÆÐ½ºÃò¾î ÁõÈıº.
  • Gradenigos syndrome
    Ãßü(÷ºÎ)¿° ÁõÈıº, ±×¶óµ¥´Ï
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
  • ¿µ¹®
    ÇѱÛ
  • orbital region
    ¾È¿ÍºÎÀ§
  • orbital region
    ´«ºÎÀ§
  • orbital region ³ª regio orbitalis
    ¾È¿ÍºÎÀ§, ¾È¿ÍºÎ.
  • orbital rim
    ¾È¿Í¿¬, ¾È¿Í°¡ÀåÀÚ¸®
  • orbital roof
    ¾È¿Í»óº®
  • orbital septum
    ¾È¿Í°Ý¸·(äÑèÀ̰د)
  • orbital septum
    ´«È®»çÀ̸·
  • orbital septum ³ª s. orbitale
    ¾È¿Í°Ý¸·(äÑèÀ̰د).
  • orbital steering
    ±ËµµÁ¶Á¤(ÏùÔ³ðàïÚ).
  • orbital sulci
    ´«È®°í¶û
  • orbital sulci ³ª s. orbitales
    ¾È¿Í°í¶û, ¾È¿Í±¸(äÑèÀϵ).
  • orbital surface
    ¾È¿Í¸é(äÑèÀØü).
  • orbital surface
    ´«È®¸é
  • orbital tumor
    ¾È¿ÍÁ¾¾ç
  • orbital valency
    ±Ëµµ¿øÀÚ°¡(ÏùÔ³ê«í­Ê¤).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 7
GS gallstone; Gardner syndrome; gastric shield; general surgery; gestational score; Gilbert syndrome; g...
HSS Hallermann-Streiff syndrome; Hallervorden-Spatz syndrome; Henoch-Schonlein syndrome; high-speed supe...
MAS magic angle spinning; Manifest Anxiety Scale; maximum average score; McCune-Albright syndrome; mecon...
MDS Master of Dental Surgery; maternal deprivation syndrome; medical data screening; medical data system...
OHS obesity hypoventilation syndrome; occipital Horn syndrome; occupational health service; ocular histo...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 7
APS I Autoimmune polyendocrine syndrome type I
APS-1 Autoimmune polyglandular syndrome type 1
BBS BARDET-Biedl syndrome
BLS Bare Lymphocyte Syndrome
BS Bartter syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • burning feel syndrome
    ÀÛ¿­°¨ ÁõÈıº, ¼ÒÀÛÁ· ÁõÈıº
  • Bäfverstedt's syndrome
    º£Æä¸£½ºÅׯ® ÁõÈıº
  • capillary leak syndrome
    ¸ð¼¼Ç÷°ü ´©Ãâ ÁõÈıº
  • caplans syndrome
    ijÀÌÇöõ ÁõÈıº
  • carcinoid syndrome
    Ä«¸£½Ã³ëÀ̵å ÁõÈıº
  • cardiofaciocutaneous syndrome
    ½ÉÀå-¾ó±¼-ÇǺΠÁõÈıº
  • carotid artery syndrome
    °æµ¿¸Æ ÁõÈıº
  • carotid sinus syndrome
    °æµ¿¸Æµ¿ ÁõÈıº
  • 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
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
Ahumada-Del Castillo syndrome <syndrome> Unphysiological lactation and amenorrhoea not following pregnancy characterised by hyperprolactinaemia and a pituitary adenoma.
Synonym: Argonz-Del Castillo syndrome.
(05 Mar 2000)
Aicardi's syndrome <syndrome> Agenesis of the corpus collosum with infantile spasms in female babies.
(05 Mar 2000)
alagille syndrome <syndrome> Hypoplasia of the hepatic ducts, congenital pulmonary artery stenosis, facial abnormalities, and other congenital malformations, particularly skeletal. It is often presented as jaundice during the neonatal period. It is an autosomal recessive disease generally manifesting during childhood. "arteriohepatic" refers to the pulmonary artery and the intrahepatic bile ducts, not to the hepatic artery.
(12 Dec 1998)
Albright's syndrome <syndrome> A condition of cystic bone growth that results from abnormal bone development. May occur with bone lesions, skin pigmentation and endocrine abnormalities.
See: McCune-Albright syndrome.
(27 Sep 1997)
alcohol amnestic syndrome <syndrome> An amnestic syndrome resulting from alcoholism; alcoholic "blackouts." Cf.: Korsakoff's syndrome.
(05 Mar 2000)
Aldrich syndrome <syndrome> An sex-linked (X chromosome) genetic disorder occurring in male children that is characterised by thrombocytopenia, eczema, melena and susceptibility to bacterial infections. Death often occurs from severe haemorrhage or overwhelming sepsis.
Inheritance: sex-linked (X chromosome).
(27 Sep 1997)
Alezzandrini's syndrome <syndrome> A rare syndrome appearing in adolescents and young adults, characterised by unilateral degenerative retinitis, followed by ipsilateral poliosis and facial vitiligo, and occasionally bilateral perceptive deafness.
(05 Mar 2000)
Alice in Wonderland syndrome <syndrome> The illusion of dreams, feelings of levitation, and alteration in the sense of the passage of time, sometimes associated with migraine, epilepsy, and various diseases of the parietal lobe of the brain.
(05 Mar 2000)
Allen-Masters syndrome <syndrome> Pelvic pain resulting from an old laceration of the broad ligament received during delivery.
(05 Mar 2000)
Alpert syndrome <syndrome> A usually inherited disorder characterised by premature closing of the cranial suture lines resulting in a peaked shaped head and abnormal facial appearance. Since it is usually autosomal dominant one or both parents also have the disorder.
Surgery is used to correct skull and facial abnormalities.
Inheritance: autosomal dominant.
(27 Sep 1997)
Alport's syndrome <syndrome> Progressive microscopic haematuria leading to chronic renal failure earlier in males, accompanied by defects such as sensorineural hearing loss, lenticonus, and maculopathy; autosomal dominant, autosomal recessive, and X-linked forms known.
(05 Mar 2000)
Alport syndrome <syndrome> An uncommon inherited disorder involving damage to the kidneys, haematuria and hearing loss. In some individuals vision may also be affected.
Symptoms include loss of hearing, abnormal colour to urine, swelling, cough and decline in vision.
Incidence: 1 in 50,000.
Inheritance: sex-linked autosomal dominant.
(15 Nov 1997)
Alstrom's syndrome <syndrome> Retinal degeneration with nystagmus and loss of central vision, associated with obesity in childhood; sensorineural hearing loss and diabetes mellitus usually occur after age 10; autosomal recessive inheritance.
(05 Mar 2000)
amenorrhoea-galactorrhoea syndrome <syndrome> Unphysiologic lactation from endocrinological causes or from a pituitary tumour.
(05 Mar 2000)
amnestic syndrome <syndrome> May occur as a sequel to chronic alcohol abuse. Features include personality changes, confabulation, psychosis, disorientation, polyneuritis, insomnia and hallucinations.
(27 Sep 1997)
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