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"epidermolysis bullosa, dermal type"¿¡ ´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
  • hyperplastic epidermolysis bullosa
    Áõ½Ä¹°ÁýÇ¥Çǹڸ®Áõ
  • epidermolysis
    Ç¥Çǹڸ®(Áõ)
  • combustio bullosa
    ¹°Áý¿­»ó
  • concha bullosa
    ÁָӴϼ±¹ÝÁõ
  • impetigo bullosa
    ¹°Áý°í¸§µüÁöÁõ, ¼öÆ÷³ó°¡Áø
  • dermal
    1. ÇǺÎ- 2. ÁøÇÇ-
  • dermal arterial network
    ÁøÇǵ¿¸Æ±×¹°, ÁøÇǵ¿¸Æ¸Á
  • dermal hypersensitivity
    ÇǺΰú¹Î¼º
  • dermal melanocytic nevus
    ÁøÇǸá¶ó´Ñ¼¼Æ÷¸ð¹Ý
  • dermal melanocytosis
    ÁøÇǸá¶ó´Ñ¼¼Æ÷Áõ
  • dermal papilla
    ÁøÇÇÀ¯µÎ
  • dermal ridge
    ÁøÇǴɼ±
  • dermal sinus
    ÇǺα¼, ÇǺε¿
  • focal dermal hypoplasia
    ±¹¼ÒÁøÇÇÇü¼ºÀúÇÏÁõ
  • asthenic type
    ¹«·ÂüÇü
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 10 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dermal
    ÇǺÎ-, ÁøÇÇ-
  • epidermolysis
    Ç¥Çǹڸ®Áõ
  • tension type headache
    ±äÀåÇüµÎÅë
  • storage-type
    ÃàÀûÇü
  • type
    Çü, À¯Çü
  • blood type
    Ç÷¾×Çü
  • Borrmann type
    º¸¸£¸¸Çü
  • cellular type
    ¼¼Æ÷Çü
  • lepromatous type
    ³ªÁ¾Çü
  • scirrhous type
    °æÈ­Çü
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hyperplastic epidermolysis bullosa
    Áõ½Ä¹°ÁýÇ¥Çǹڸ®Áõ
  • recessive dystrophic epidermolysis bullosa
    ¿­¼ºÀ§Ã๰ÁýÇ¥Çǹڸ®Áõ
  • epidermolysis
    Ç¥Çǹڸ®Áõ
  • hereditary bullous epidermolysis
    À¯Àü¹°ÁýÇ¥Çǹڸ®Áõ
  • combustio bullosa
    ¹°Áý¿­»ó
  • concha bullosa
    ÁָӴϼ±¹Ý
  • impetigo Bullosa
    (¢¡bullous impetigo) ¹°Áý°í¸§µüÁöÁõ
  • dermal
    ÇǺÎ-, ÁøÇÇ-
  • dermal hypersensitivity
    ÇǺΰú¹Î
  • dermal melanocytosis
    ÁøÇǸá¶ó´Ñ¼¼Æ÷Áõ
  • dermal papilla
    ÁøÇÇÀ¯µÎ
  • dermal ridge
    ÁøÇǴɼ±
  • dermal sensation
    ÇǺΰ¨°¢
  • dermal sinus
    ÇǺα¼
  • dermal arterial network
    ÁøÇǵ¿¸Æ±×¹°
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • 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
  • hereditary bullous epidermolysis ³ª e.bullosa hereditaria
    À¯Àü¼º Ç¥ÇǼöÆ÷Áõ.
  • hyperplastic epidermolysis bullosa
    °úÇü¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • recessive dystrophic epidermolysis bullosa
    ¿­¼º ¿µ¾çÀå¾Ö ¼öÆ÷ Ç¥Çǹڸ®Áõ
  • Goltzs syndrome => focal dermal hypoplasia
    ±¹¼Ò ÁøÇÇ Çü¼ººÎÀüÁõ
  • porokeratotoic eccrine ostial and dermal duct nevus
    ÇѰø°¢È­Áõ¼º ¿¡Å©¸°±¸¸Û ¹× ÁøÇǰü¸ð¹Ý
  • primary dermal ridge
    ÀÏÂ÷ÁøÇǸª(ìéó­òØ ù«×Ò).
  • generalized nonmutilating ausomal recessive dystrophic epidermolysis b
    Àü½Å¼º ºñÀý´Ü¼º »ó¿°»öü ¿­¼º ÀÌ¿µ¾ç¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • Ichthyosis bullosa of Siemens
    Áö¸à½º ¼öÆ÷¼º ¾î¸°¼±
  • impetigo bullosa ³ª
    ´ë¼öÆ÷¼º ³ó°¡Áø(ÓÞâ©øÞàõÒÛʲòÖ)
  • impetigo contagiosa bullosa ³ª
    Àü¿°¼º´ë¼öÆ÷¼º³ó°¡Áø(îîæøàõÓÞâ©øÞàõÒÛʲòÖ)
  • photodermatitis bullosa striata
    ¼±»ó ¼öÆ÷¼º ±¤ÇǺο°
  • purpura bullosa
    ´ë¼öÆ÷¼º(ÓÞâ©øÜàõ) ÀÚ¹Ý.
  • purpura bullosa
    ´ë¼öÆ÷¼º ÀÚ¹Ý(ÓÞâ©øÜàõ í¹Úè)
¿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 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
  • generalized autosomal recessive dystrophic epidermolysis bullosa
    Àü½Å¼º »ó¿°»öü ¿­¼º ÀÌ¿µ¾ç¼º ¼öÆ÷¼º Ç¥Çǹڸ®Áõ
  • hereditary bullous epidermolysis ³ª e.bullosa hereditaria
    À¯Àü¼º Ç¥ÇǼöÆ÷Áõ.
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Deep dermal venous plexus
    ±íÀºÁøÇÇÁ¤¸Æ¾ó±â
    [¿¾ ¿ë¾î] ½ÉÁøÇdz»Á¤¸ÆÃÑ
  • Dermal groove
    ÁøÇǰí¶û
    [¿¾ ¿ë¾î] Á¶ÁøÇDZ¸
  • Dermal abundance (Scleroderm)
    ÁøÇǰú´Ù (ÇǺΰæÈ­Áõ)
    [¿¾ ¿ë¾î] ¿ÜÇǰú´Ù
  • Dermal crest
    ÁøÇǴɼ±
    [¿¾ ¿ë¾î] Á¶ÁøÇǸª
  • Dermal arterial network
    ÁøÇǵ¿¸Æ±×¹°
    [¿¾ ¿ë¾î] ÁøÇǵ¿¸Æ¸Á
  • Dermal root sheath
    ÁøÇǻѸ®Áý
    [¿¾ ¿ë¾î] ÁøÇǼº±ÙÃÊ
  • Capillary network of dermal root sheath
    ÁøÇǻѸ®Áý¸ð¼¼Ç÷°ü±×¹°
    [¿¾ ¿ë¾î] ÁøÇǼº±ÙÃʸð¼¼Ç÷°ü¸Á
  • Dermal nerve plexus
    ÁøÇǽŰæ¾ó±â
    [¿¾ ¿ë¾î] ÁøÇǽŰæÃÑ
  • Dermal papilla
    ÁøÇÇÀ¯µÎ
    [¿¾ ¿ë¾î] ÁøÇÇÀ¯µÎ
  • Dermal sheath of hair
    ÅÐÁøÇÇÁý
    [¿¾ ¿ë¾î] ¸ðÁøÇÇÃÊ
  • Chief cell [Type I glomus cell]
    °ú¸³¼¼Æ÷
    [¿¾ ¿ë¾î] ÁÖ¼¼Æ÷(Á¦1Çü»ç±¸¼¼Æ÷)
  • Regular type
    ±ÔÄ¢Çü
    [¿¾ ¿ë¾î] ±ÔĢġ¹Ð°áÇÕÁ¶Á÷
  • Muscular type of artery
    ±ÙÀ°Çüµ¿¸Æ
    [¿¾ ¿ë¾î] ±ÙÇüµ¿¸Æ
  • Muscular type of lymphatic vessel
    ±ÙÀ°Çü¸²ÇÁ°ü
    [¿¾ ¿ë¾î] ±ÙÇüÀӯİü
  • Muscular type of vein
    ±ÙÀ°ÇüÁ¤¸Æ
    [¿¾ ¿ë¾î] ±ÙÇüÁ¤¸Æ
´ëÇѱâ»ýÃæÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • polymyarian type
    ´Ù±ÙÀ°Çü
  • type specimen
    ±âÁØÇ¥º»
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • ABO blood group (type) system
    ABOÇ÷¾×Çü (úìäûúþ) ½Ã½ºÅÛ
  • C-type particles
    C-Çü(û¡) ÀÔÀÚ(Ø£í­)
  • C-type virus
    "C-Çü(û¡) ¹ÙÀÌ·¯½º, (ÔÒ) C-type particles"
  • dehydrogenase-type mechanism
    µðÇÏÀ̵å·ÎÀú³×À̽ºÇü(úþ) ±âÀü(Ѧï®)
  • delayed-type hypersensitivity
    Áö¿¬Çü °ú¹ÎÁõ(òÀæÅû¡Î¦ÚÂñø)
  • immediate-type hypersensitivity
    Áï½ÃÇü °ú¹ÎÁõ(ñíãÁúþΦÚÂñø)
  • L-type structure
    L-Çü(úþ)±¸Á¶(ϰðã)
  • mixed-type inhibitor
    È¥ÇÕÇü ÀúÇØÁ¦(ûèùêúþîÁúªð¥)
  • plant-type ferredoxin
    ½Ä¹°Çü(ãÕÚªû¡) Æä·¹µ¶½Å
  • plaque-type mutant
    ÇöóÅ©Çü(û¡) º¯ÀÌü(ܨì¶ô÷)
  • transaminase-type mechanism
    Æ®¶õ½º¾Æ¹Ì³×À̽ºÇü (úþ) ±âÀü(Ѧï®)
  • type A hepatitis
    AÇü(úþ) °£¿°(ÊÜæú)
  • type A RNA virus
    AÇü(úþ) RNA ¹ÙÀÌ·¯½º
  • type B hepatitis
    BÇü(úþ) °£¿°(ÊÜæú)
  • type B RNA virus
    BÇü(úþ) RNA ¹ÙÀÌ·¯½º
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 9 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dermal
    ÇǺÎÀÇ, ÁøÇÇÀÇ
  • urticaria bullosa
    ¼öÆ÷¼ºµÎµå·¯±â
  • bell type
    Á¾¸ð¾ç, Á¾Çü
  • intracanalicular type
    ¼Ò°ü³»Çü
  • mobile type diagnostic X ray apparatus
    À̵¿Çü Áø´ÜX¼±ÀåÄ¡
  • onion-skin type
    ¾çÆÄ²®Áú¸ð¾ç
  • phased linear array type
    À§»óÂ÷¼±Çü¹è¿­½Ä
  • RF coil type
    °íÁÖÆÄÄÚÀÏÀ¯Çü
  • split electrode type probe
    ºÐÇÒÀü±ØÅ½ÃËÀÚ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
EBA epidermolysis bullosa acquisita; epidermolysis bullosa atrophicans; orthoethoxybenzoic acid
ECG Electro-Cardio-Graphy(-Gram); ½ÉÀüµµ
   = EKG
  1. Conducting System Structu...
EBDCT Cockayne-Touraine type of epidermolysis bullosa dystrophica
PMD Progressive Muscular Dystrophy; ÁøÇ༺ ±ÙÀÌ¿µ¾çÁõ
  Types of PMD(Progressive Muscular Dystroph...
DEB diepoxybutane; diethylbutanediol; Division of Environmental Biology; dystrophic epidermolysis bullos...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
DEB Dystrophic Epidermolysis Bullosa
EB Epidermolysis Bullosa
EBS Epidermolysis Bullosa Simplex
EBA Epidermolysis bullosa acquisita
GABEB Generalised atrophic benign epidermolysis bullosa
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • dystrophic epidermolysis bullosa
    ÀÌ¿µ¾ç¼º ¼öÆ÷¼º Ç¥Çǹڸ®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
  • dendritic dermal melanocyte
    ¼öÁö»ó ÁøÇÇ ¸á¶ó´Ñ ¼¼Æ÷
  • dermal
    ÇǺÎÀÇ, ÁøÇÇÀÇ
  • dermal hypoplasia
    ÁøÇÇ Çü¼º ºÎÀüÁõ
  • dermal melanocytic nevus
    ÁøÇÇ ¸á¶ó´Ñ ¼¼Æ÷ ¸ð¹Ý
  • dermal pattern
    ÁøÇÇÇü
  • dermal respiration
    ÇǺΠȣÈí
  • dermal sense
    ÇǺΠ°¨°¢
  • epidermolysis acquisita
    ÈÄõ¼º Ç¥ÇÇ ¹Ú¸®Áõ, ÈÄõ¼º Ç¥ÇÇ ¼öÆ÷Áõ
  • acantholysis bullosa acquisita
    ÈÄõ¼º ¼öÆ÷¼º ±Ø¼¼Æ÷ ºÐ¸®
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
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)
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)
concha bullosa Abnormal pneumatization of the middle turbinate which may interfere with normal ventilation of sinus ostia and can result in recurrent sinusitis.
(05 Mar 2000)
Pseudostertagia bullosa One of the medium stomach worms located in the abomasum of sheep, goats, and pronghorn; it is found chiefly in the western U.S.
(05 Mar 2000)
impetigo bullosa Impetigo with lesions of large size, forming bullae.
(05 Mar 2000)
impetigo contagiosa bullosa Discrete purulent skin lesions occasionally seen with streptococcal pyoderma.
(05 Mar 2000)
urticaria bullosa An eruption of wheals capped with subepidermal vesicles.
Synonym: urticaria vesiculosa.
(05 Mar 2000)
post-kala azar dermal leishmanoid A chronic, progressive, granulomatous, nonulcerating hypopigmented nodular cutaneous outbreak that may appear 6 months to 5 years after spontaneous or drug cure of visceral leishmaniasis (kala azar); this condition was first described in India and is most characteristic of kala azar in that country.
Synonym: dermal leishmanoid.
(05 Mar 2000)
dermal 1. Pertaining to the integument or skin of animals; dermic; as, the dermal secretions.
2. <anatomy> Pertaining to the dermis or true skin.
Origin: From Derm.
Source: Websters Dictionary
(01 Mar 1998)
dermal bone A bone formed by ossification of the cutis.
(05 Mar 2000)
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dermal
    ÇǺο¡ °üÇÑ
  • type
    Çü,ŸÀÌÇÁ,ÀüÇü,ȰÀÚ,ÀÚü
  • C-type virus
    CÇü ¹ÙÀÌ·¯½º(¹ß¾Ï¼ºÀ¸·Î ¿©°ÜÁö°í ÀÖÀ½)
  • Gothic type
    °íµñ ȰÀÚü
  • Moon type
    (¿µ±¹ÀÎ °í¾ÈÀÚ À̸§¿¡¼­)¹®Å¸ÀÌÇÁ(¹®ÀÚ ½ÀµæÈÄÀÇ ½Ç¸íÀÚ¸¦ À§ÇÑ µµµå¶óÁø ¹®ÀÚÀÇ ¼­Ã¼,Àμâ¹ý)
  • Moon type
    ¸ÍÀοëÀÇ ¹®½Ä¼±ÀÚ(¿µ±¹ÀÎ W,Moon ¹ß¸í)
  • Roman letters(type)
    ·Î¸¸Ã¼(ȰÀÚ)
  • character type
    ¼º°Ý À¯Çü
  • cold type
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