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"hereditary bullous epidermolysis"¿¡ ´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
  • epidermolysis
    Ç¥Çǹڸ®(Áõ)
  • hyperplastic epidermolysis bullosa
    Áõ½Ä¹°ÁýÇ¥Çǹڸ®Áõ
  • aphakic bullous keratopathy
    ¹«¼öÁ¤Ã¼¹°Áý°¢¸·º´(Áõ), ¹«¼öÁ¤Ã¼¼öÆ÷°¢¸·º´(Áõ)
  • bullous
    ¹°Áý-
  • bullous dermatitis
    ¹°ÁýÇǺο°
  • bullous dermatosis
    ¹°ÁýÇǺκ´
  • bullous detachment
    ¼öÆ÷¹Ú¸®
  • bullous emphysema
    Å«°ø±âÁýÆó°ø±âÁõ, ¼öÆ÷¼ºÆó±âÁ¾
  • bullous eruption
    Å«¹°Áý¹ßÁø
  • bullous follicular keratosis
    ¹°ÁýÅÐÁý°¢È­Áõ, ¼öÆ÷¸ð³¶°¢È­Áõ
  • bullous impetigo
    ¹°Áý°í¸§µüÁöÁõ, ¼öÆ÷³ó°¡Áø
  • bullous keratitis
    ¹°Áý°¢¸·¿°
  • bullous keratopathy
    ¹°Áý°¢¸·º´(Áõ), ¼öÆ÷°¢¸·º´(Áõ)
  • bullous mastocytosis
    ¹°Áýºñ¸¸¼¼Æ÷Áõ
  • bullous pemphigoid
    ¹°ÁýÀ¯»çõÆ÷â, ¹°ÁýÀ¯»ç¹°ÁýÁõ
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  • ¿µ¹®
    ÇѱÛ
  • epidermolysis
    Ç¥Çǹڸ®Áõ
  • hereditary
    À¯Àü-
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´Áõ
  • hereditary spherocytosis
    À¯ÀüµÕ±ÙÀûÇ÷±¸Áõ, À¯Àü±¸ÇüÀûÇ÷±¸Áõ
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  • ¿µ¹®
    ÇѱÛ
  • hereditary bullous epidermolysis
    À¯Àü¹°ÁýÇ¥Çǹڸ®Áõ
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  • ¿µ¹®
    ÇѱÛ
  • epidermolysis
    Ç¥Çǹڸ®Áõ
  • hyperplastic epidermolysis bullosa
    Áõ½Ä¹°ÁýÇ¥Çǹڸ®Áõ
  • recessive dystrophic epidermolysis bullosa
    ¿­¼ºÀ§Ã๰ÁýÇ¥Çǹڸ®Áõ
  • aphakic bullous keratopathy
    ¹«¼öÁ¤Ã¼¹°Áý°¢¸·º´Áõ
  • bullous
    ¹°Áý-
  • bullous dermatitis
    ¹°ÁýÇǺο°
  • bullous dermatosis
    ¹°ÁýÇǺκ´
  • bullous detachment
    ¼öÆ÷¹Ú¸®
  • bullous eruption
    Å«¹°Áý¹ßÁø
  • bullous impetigo
    ¹°Áý°í¸§µüÁöÁõ
  • bullous keratitis
    ¹°Áý°¢¸·¿°
  • bullous keratopathy
    ¹°Áý°¢¸·º´Áõ
  • bullous mastocytosis
    ¹°Áýºñ¸¸¼¼Æ÷Áõ
  • bullous purpura
    ¼öÆ÷ÀÚ»ö¹Ý, ¹°ÁýÀÚ»ö¹Ý
  • bullous follicular keratosis
    ¼öÆ÷¸ð³¶°¢È­Áõ, ¹°ÁýÅÐÁý°¢È­Áõ
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  • ¿µ¹®
    ÇѱÛ
  • hereditary bullous epidermolysis ³ª e.bullosa hereditaria
    À¯Àü¼º Ç¥ÇǼöÆ÷Áõ.
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • aphakic bullous keratopathy
    ¹«¼öÁ¤Ã¼¼öÆ÷°¢¸·º´Áõ
  • Herlitz disease => generalized junctinal epidermolysis bullosa
    Àü½Å¼º °æ°è¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • generalized autosomal recessive dystrophic epidermolysis bullosa
    Àü½Å¼º »ó¿°»öü ¿­¼º ÀÌ¿µ¾ç¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • generalized nonmutilating ausomal recessive dystrophic epidermolysis b
    Àü½Å¼º ºñÀý´Ü¼º »ó¿°»öü ¿­¼º ÀÌ¿µ¾ç¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • hyperplastic epidermolysis bullosa
    °úÇü¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • recessive dystrophic epidermolysis bullosa
    ¿­¼º ¿µ¾çÀå¾Ö ¼öÆ÷ Ç¥Çǹڸ®Áõ
  • Hereditary camptodactyly
    À¯Àü¼º ±¼ÁöÁõ
  • hearing loss, congenital hereditary
    ¼±Ãµ(¼º) À¯Àü¼º ³­Ã»
  • hereditary
    À¯Àü¼ºÀÇ
  • hereditary adrenogenital syndrome
    À¯Àü¼º ºÎ½Å¼º±â¼º ÁõÈıº.
  • hereditary angioedema
    À¯Àü¼º ¸Æ°üºÎÁ¾
  • hereditary angioedema
    À¯Àü¼ºÇ÷°üºÎÁ¾
  • hereditary aphasia
    À¯Àü(¼º) ½Ç¾î(Áõ).
  • hereditary ataxia
    À¯Àü(¼º) ¿îµ¿½ÇÁ¶.
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¼º ¾ç¼º »óÇdz» ÀÌ»ó°¢È­Áõ
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  • ¿µ¹®
    ÇѱÛ
  • hereditary bullous epidermolysis ³ª e.bullosa hereditaria
    À¯Àü¼º Ç¥ÇǼöÆ÷Áõ.
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemen
    »ó¿°»öü ¿­¼º ÀÌ¿µ¾ç¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • dominant dystrophic epidermolysis bullosa
    ¿ì¼º ÀÌ¿µ¾ç¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • dystrophic epidermolysis bullosa
    ÀÌ¿µ¾ç¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • epidermolysis
    Ç¥Çǹڸ®Áõ
  • epidermolysis acquisita<³ª>
    ÈÄõ¼º Ç¥Çǹڸ®Áõ
  • epidermolysis bullosa
    ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • epidermolysis bullosa
    ¼öÆ÷¼ºÇ¥ÇÇ ¹Ú¸®Áõ(â©øÞàõøúù«ÚÎ×îñø)
  • epidermolysis bullosa atrophicans
    À§Ã༺ ¼öÆ÷ Ç¥Çǹڸ®Áõ
  • epidermolysis bullosa hereditaria simplex<³ª>
    ´Ü¼ø¼±Ãµ¼º ¼öÆ÷ Ç¥Çǹڸ® Áõ
  • epidermolysis bullosa hereditaria<³ª>
    ¼±Ãµ¼º ¼öÆ÷ Ç¥Çǹڸ®Áõ
  • epidermolysis bullosa letalis
    Ä¡»ç¼º ¼öÆ÷ Ç¥Çǹڸ®Áõ
  • epidermolysis bullosa neurotrophica
    ½Å°æ¿µ¾ç¼º ¼öÆ÷ Ç¥Çǹڸ®Áõ
  • epidermolysis bullosa progressiva
    ÁøÇ༺ ¼öÆ÷ Ç¥Çǹڸ®Áõ
  • epidermolysis bullosa simplex
    ´Ü¼ø¼º ¼öÆ÷ Ç¥Çǹڸ®Áõ
  • epidermolysis bullosa<³ª>
    ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
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  • ¿µ¹®
    ÇѱÛ
  • hereditary code
    À¯Àü ºÎÈ£(ë¶îîݬûÜ)
  • hereditary material
    À¯Àü ¹°Áú(ë¶îîÚªòõ)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 6 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • bullous
    ¼öÆ÷¼ºÀÇ
  • hereditary
    À¯Àü¼ºÀÇ
  • hereditary craniofacial dysostosis
    À¯Àü¼ºµÎ°³¾È¸éÀ̰ñÁõ
  • hereditary disease
    À¯Àüº´
  • hereditary ectodermal polydysplasia
    À¯Àü¼º¿Ü¹è¿±¼º´Ù¹ßÀÌÇü¼ºÁõ
  • hereditary hemorrhagic telangiectasia
    À¯Àü¼ºÃâÇ÷¼º¸ð¼¼Ç÷°üÈ®Àå
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
EBA epidermolysis bullosa acquisita; epidermolysis bullosa atrophicans; orthoethoxybenzoic acid
BP   1) Blood Pressure; Ç÷¾Ð
  2) Bullous Pemphigoid
  3) Benzathin P...
ABK aphakic bullous keratopathy
BIE bullous ichthyosiform erythroderma
BP Bachelor of Pharmacy; back pressure; barometric pressure; basic protein; bathroom privileges; bed pa...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
BPAG1 Bullous Pemphigoid Antigen 1
BP Bullous pemphigoid
BPA Bullous pemphigoid antigen
BPAG2 Bullous pemphigoid antigen 2
CBDC Chronic bullous dermatosis of childhood
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • dystrophic epidermolysis bullosa
    ÀÌ¿µ¾ç¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • epidermolysis acquisita
    ÈÄõ¼º Ç¥ÇÇ ¹Ú¸®Áõ, ÈÄõ¼º Ç¥ÇÇ ¼öÆ÷Áõ
  • epidermolysis bullosa acquisita
    ÈÄõ¼º Ç¥ÇÇ ¼öÆ÷Áõ, ÈÄõ¼º ¼öÆ÷¼º Ç¥ÇÇ ¹Ú¸®Áõ
    1. ¼öÆ÷¿Í ¼ÒÆ÷ÁøÀÇ ¹ß»ýÀ» Ư¡À¸·Î ÇÏ´Â À¯Àü¼º ÇǺκ´ ±º. 2. ¼º³â¿¡ ½ÃÀÛÇÏ¸ç ¿Ü»óÀ» ¹ÞÀº ºÎÀ§¿¡ À§Ã༺ ¹ÝÈçÀ» ³²±â´Â ¼öÆ÷°¡ »ý±ä´Ù. ¼Õ, ¹ß¿¡ Àß »ý±â¸ç µå¹°°Ô ±¸°­À» ħ¹üÇÑ´Ù. 3. ¸²ÇÁ Áõ½Ä¼º Áúȯ, Crohn º´, ±Ë¾ç¼º ´ëÀå¿°, ·ù¸¶Æ¼½º °üÀý¿°°ú µ¿¹ÝµÇ±âµµ ÇÑ´Ù. Ç¥ÇÇÇÏ ¼öÆ÷·Î ³ªÅ¸³ª¸ç ¿°Áõ ¼¼Æ÷ ħÀ±Àº ´ÜÇÙ±¸, Áß¼º±¸ ¿Ü¿¡ È£»ê±¸°¡ ÈçÈ÷ º¸ÀδÙ.
  • epidermolysis bullosa hereditaria
    ¼±Ãµ¼º ¼öÆ÷¼º Ç¥ÇÇ ¹Ú¸®Áõ
  • epidermolysis bullosa hereditaria simplex
    ´Ü¼ø ¼±Ãµ¼º ¼öÆ÷¼º Ç¥ÇÇ ¹Ú¸®Áõ
  • epidermolysis bullosa simplex
    ´Ü¼ø¼º ¼öÆ÷¼º Ç¥ÇÇ ¹Ú¸®Á¾
    »ó¿°»öü ¿ì¼º À¯ÀüÀ» ÇÏ¸ç ¼Õ, ¹ßÀ» À§½ÃÇÑ ÆÈ²ÞÄ¡, ¹«¸­ µîÀÇ °üÀýÀ̳ª ¹Ýº¹ÇÏ¿© ¿Ü»óÀ» ¹ÞÀº ºÎÀ§¿¡ Å©°í ÀÛÀº ¼öÆ÷°¡ ¹ß»ýÇϸç À§Ã༺ ¹ÝÈçÀ» ³²±âÁö ¾Ê´Â´Ù. º´¼Ò´Â º¸Åë »ýÈÄ 1³â À̳»¿¡ ½ÃÀÛÇÑ´Ù. ¹ß»ý ÃʱâÀÇ º´¼Ò¿¡¼­´Â ±âÀú ¼¼Æ÷ÀÇ °øÆ÷È­°¡ º¸À̰í ÀÌ¿¡ µû¶ó ÀÏÂ÷Àû ¹Ú¸®´Â ±âÀú¼¼Æ÷Ãþ »óºÎ ȤÀº ÀÌÀÇ º¯¼ºÀ¸·Î ÀÎÇÏ¿© Ç¥ÇÇ ÇϺο¡ ³ªÅ¸³­´Ù. PAS ¾ç¼ºÀÎ ±âÀú¸·Àº ¼öÆ÷ ¾Æ·¡ÀÇ ÁøÇÇ¿¡ ºÎÂøµÇ¾î ÀÖ´Ù.
  • junctional epidermolysis bullosa
    ¿¬Á¢ºÎ ¼öÆ÷¼º Ç¥ÇÇ ¹Ú¸®Áõ
  • aphakic bullous keratopathy
    ¹«¼öÁ¤Ã¼ ¼öÆ÷ °¢¸·º´Áõ
  • bullous
    ¼öÆ÷Çü, ¼öÆ÷¼º, Å« ¼öÆ÷¼º
    ¼öÆ÷¿¡ °üÇÑ °ÍÀ̳ª ¼öÆ÷°¡ Ư¡ÀÎ.
  • bullous congenital icthyosiform erythroderma
    ¼öÆ÷¼º ¼±Ãµ¼º ¾î¸°¼±»ó È«ÇÇÁõ
  • bullous disease
    ¼öÆ÷¼º Áúȯ
  • bullous drug-induced exanthema
    ¾à¹°¿¡ ÀÇÇÑ ¼öÆ÷¼º ¹ßÁø
  • bullous lesion
    ¼öÆ÷¼º º´¼Ò
  • bullous pemphigoid
    ¼öÆ÷¼º À¯ÃµÆ÷â
    1. ÇǺγª Á¡¸·ÀÇ ±âÀú¸·´ë¿¡ ´ëÇÑ Ig G, IgE ÇüÀÇ ÀÚ°¡ Ç×ü¸¦ °¡Áö´Â ÀÚ°¡ ¸é¿ª Áúȯ. 2. »óÇÇ ±âÀú¸·ÀÇ Åõ¸íÆÇ³»¿¡ ÀÖ´Â 220Kd ´Ü¹éÁú¿¡ ´ëÇÑ ÀÚ°¡ Ç×ü°¡ Ư¡. ÀÓ»óÀûÀ¸·Î 50´ë À̻󿡼­ Á¦ÀÏ ¸ÕÀú ¹ß°ßµÇ¸ç ³²ÀÚ°¡ ¿©ÀÚº¸´Ù ¸¹ÀÌ ¹ß»ýÇϰí ÇǺΰ¡ Á¦ÀÏ ¸ÕÀú ¹ß»ýÇÏ´Â ºÎÀ§ÀÌ´Ù. ±¸°­ º´¼Ò´Â º°·Î ³ªÅ¸³ªÁö ¾ÊÀ¸¸ç ³Ð°Ô ºÐÆ÷ÇÑ´Ù. Ãʱâ Ä¡·á´Â ÄÚ¸£Æ¼ÄÚ½ºÅ×·ÎÀ̵åÀÇ ±¹¼ÒµµÆ÷ÀÌ´Ù.
  • bullous skin disease
    ¼öÆ÷¼º ÇǺΠÁúȯ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
epidermolysis A condition in which the epidermis is loosely attached to the corium, readily exfoliating or forming blisters.
Origin: epidermis + G. Lysis, loosening
(05 Mar 2000)
epidermolysis bullosa This represents a group of rare inherited disorders in which blistering of the skin occurs in response to skin trauma. Large fluid-filled blisters can occur in response to injury, skin rubbing, chafing or even increases in room temperature. Secondary bacterial infection of the blisters is common. Complications include oesophageal stricture, infections, loss of function of hands and feet and malnutrition. The dermatologist is the expert in the evaluation and treatment of this disorder.
(27 Sep 1997)
epidermolysis bullosa acquisita Form of epidermolysis bullosa characterised by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescence shows IgG deposited at the dermo-epidermal junction.
(12 Dec 1998)
epidermolysis bullosa dystrophica Form of epidermolysis bullosa characterised by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms.
(12 Dec 1998)
epidermolysis bullosa, junctional Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterised by generalised blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane.
(12 Dec 1998)
epidermolysis bullosa lethalis Epidermolysis bullosa in which the bullae are persistent, nonhealing, and often present in the oral mucosa and trachea, but not on the palms and soles, leading to death.
Synonym: epidermolysis bullosa, junctional type, Herlitz syndrome.
(05 Mar 2000)
epidermolysis bullosa simplex This represents a group of rare inherited disorders in which blistering of the skin occurs in response to skin trauma. Large fluid-filled blisters can occur in response to injury, skin rubbing, chafing or even increases in room temperature. Secondary bacterial infection of the blisters is common. Complications include oesophageal stricture, infections, loss of function of hands and feet and malnutrition. The dermatologist is the expert in the evaluation and treatment of this disorder.
(27 Sep 1997)
bullous <pathology> Pertaining to or characterised by bullae.
(18 Nov 1997)
bullous congenital ichthyosiform erythroderma Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance.
See: epidermolytic hyperkeratosis.
Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix.
(05 Mar 2000)
bullous diseases of oesophagus <radiology> Epidermolysis bullosa dystrophica, autosomal recessive, presents in infancy or later life, epidermal-dermal separation, with or without anal strictures, Treatment: conservative, soft diet, benign mucous membrane (cicatricial) pemphigoid, not pemphigus vulgaris, not bullous pemphigoid, females (2:1), elderly
(12 Dec 1998)
bullous emphysema Emphysema in which the enlarged airspaces are one to several cm in diameter, often visible on chest radiographs. Thin-walled air sacs under tension compress pulmonary tissue, either single or multiple. Sometimes amenable to surgical resection with improvement in pulmonary function.
(05 Mar 2000)
bullous fever An obsolete term for a pyogenic infection due to local trauma, that responds to antibiotic therapy; if untreated, the condition may become extensive and the patient seriously ill.
Synonym: bullous fever.
(05 Mar 2000)
bullous impetigo of newborn Usually, widely disseminated bullous lesions appearing soon after birth, caused by infection with Staphylococcus aureus.
Synonym: impetigo neonatorum, pemphigus gangrenosus.
(05 Mar 2000)
bullous keratopathy Oedema of the corneal stroma and epithelium; occurs in Fuchs' epithelial dystrophy, advanced glaucoma and iridocyclitis, and sometimes after intraocular lens implantation.
(05 Mar 2000)
bullous myringitis <pathology> An infectious disorder of the eardrum resulting in painful blisters on the surface of the tympanic membrane. Can be a feature of otitis media caused by Mycoplasma infection.
(27 Sep 1997)
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    ÇѱÛ
  • bullous
    ¼öÆ÷¼ºÀÇ
  • hereditary
    À¯Àü¼ºÀÇ; ¼¼½ÀÀÇ
  • hereditary
    À¯ÀüÀÇ;¼¼½ÀÀÇ;´ë´ëÀÇ
  • hereditary peer
    ¼¼½À ±ÍÁ·
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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  • Á¦Ç°¸í
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    ±¸ºÐ/º¸Çè±Þ¿©
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