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"X linked disease"¿¡ ´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
  • occupational disease
    Á÷¾÷º´
  • organic disease
    ±âÁúº´
  • Osgood-Schlatter disease
    ¿À½º±Â-½¶¶óÅͺ´
  • obstructive pulmonary disease
    Æó¼âÆóº´
  • Owren¡¯s disease
    ¿Àºê·»º´
  • phytanic acid storage disease
    ÇÇź»êÃàÀûº´
  • Pick disease
    ÇȺ´
  • pigeon breeder¡¯s disease
    ºñµÑ±â»çÀ°ÀÚº´
  • pandemic disease
    ¹üÀ¯Çິ
  • pneumatic hammer disease
    ¾ÐÂø°ø±âÇØ¸Óº´
  • polycystic kidney disease
    ´Ù³¶½ÅÀ庴, ¹µÁÖ¸Ó´ÏÄáÆÏº´
  • panzootic disease
    µ¿¹°¹üÀ¯Çິ
  • posttransplant lymphoproliferative disease
    À̽ÄÈĸ²ÇÁ¼¼Æ÷Áõ½Äº´
  • prenatal disease
    Ãâ»ýÀüº´
  • primary cholestatic liver disease
    ¿ø¹ß¾µ°³ÁóÁ¤Ã¼°£Áúȯ, ¿ø¹ß´ãÁóÁ¤Ã¼°£Áúȯ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
  • psychosomatic disease
    Á¤½Å½Åüº´
  • pulmonary disease
    Æóº´
  • pulseless disease
    ¹«¸Æ¹Úº´, ¹«¸Æº´
  • pyramidal disease
    ÇǶó¹Ô½Å°æ·Îº´, Ãßü½Å°æ·Îº´
  • quarantinable disease
    °Ë¿ªÁúȯ
  • rat-bite disease
    Áã¹°±âº´
  • Raynaud¡¯s disease
    ·¹À̳뺴
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
  • renal disease
    ÄáÆÏº´, ½ÅÀ庴
  • reported communicable disease
    ½Å°íµÈÀü¿°º´
  • respiratory disease
    È£Èí±âº´
  • reversible obstructive lung disease
    °¡¿ªÆó¼âÆóº´
  • rheumatic disease
    ·ù¸¶Æ¼½ºº´
  • rheumatoid disease
    ·ù¸¶Æ¼½º¸ð¾çÁúȯ
  • rice disease
    (¢¡beriberi) °¢±â
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  • ¿µ¹®
    ÇѱÛ
  • glucuronidase deficiency disease
    ±Û·çÅ¥·Î´Ïµ¥À̽º °áÇÌÁõ
  • glycogen storage disease
    ±Û¸®ÄÚ°ÕÃàÀû Áúȯ.
  • glycogen storage disease
    ´ç¿ø ÃàÀûÁúȯ(ÓØê«õëîÝòðü´)
  • glycogen storage disease
    ±Û¸®ÄÚ°ÕÃàÀûÁúȯ
  • graft versus host disease
    ´ë¼÷ÁÖÀÌ½ÄÆíÁúȯ
  • graft versus host disease
    ÀÌ½ÄÆí´ë¼÷ÁÖº´.
  • graft versus host disease
    ÀÌ½ÄÆí´ë¼÷ÁÖº´
  • graft-versus-host disease
    ÀÌ½ÄÆí´ë¼÷ÁÖº´
  • graft-versus-host disease
    ÀÌ½ÄÆí´ë ¼÷ÁÖº´
  • granulomatous disease
    À°¾ÆÁ¾¼º Áúȯ.
  • granulomatous disease
    À°¾ÆÁ¾¼º Áúȯ
  • granulomatous disease of childhood
    ¼Ò¾ÆÀ°¾ÆÁ¾¼º Áúȯ.
  • granulomatous disease of childhood
    ¼Ò¾Æ À°¾ÆÁ¾¼º Áúȯ
  • graves disease
    ±×·¹À̺꽺 º´, Grave º´
  • grinder s disease ; silicosis
    ±ÔÆóÁõ, ºÐ¼â±â°øº´.
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
  • diffuse collagen disease
    ¹Ì¸¸¼º ±³¿øº´.
  • diffuse interstitial pulmonary disease
    ¹Ì¸¸¼º °£Áú¼º ÆóÁúȯ
  • digestive tract disease
    ¼ÒÈ­°üÁúȯ.
  • digestive tract disease
    ¼ÒÈ­±â°èÅëÁúȯ.
  • digestive tract disease
    ¼ÒÈ­±â°èÅëÁúȯ.
  • disease
    º´(º´), Áúº´(Áúº´), Áúȯ(Áúȯ).
  • disease
    Áúº´(Ü»), Áúȯ(òðü´)
  • disease
    º´, Áúº´, Áúȯ
  • disease
    º´(Ü»), Áúº´(òðÜ»), Áúȯ(òðü´).
  • disease
    º´(ËÓ), Áúº´(̤ËÓ), Áúȯ(̷̤).
  • disease carrier
    º´¿ø(ü)º¸À¯ÀÚ(Ü»êÂô÷ÜÁêóíº).
  • disease carrier
    º´¿ø(ü)º¸À¯ÀÚ(ËÓËô̧ËÓËôËö).
  • disease control
    Áúº´°ü¸®.
  • disease detection
    Áúº´¹ß°ß.
  • disease entity
    Áúº´´ÜÀ§(òðܻӤêÈ).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
XLMR X-linked mental retardation
XLMTM X-linked myotubular myopathy
XLP X-linked lymphoproliferative [syndrome]
XLR X-linked recessive
XLS X-linked recessive lymphoproliferative syndrome
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
BD Beccet disease
BBD Benign Breast Disease
BD Binswanger disease
bNED Biochemical no evidence of disease
BFD Blackfoot disease
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • Schilder's disease
    ½¯´õº´
    1. 1912³â¿¡ ±âÀçÇÑ ¼Ò¾Æ ¹× ÀþÀºÀÌ¿¡°Ô ÀϾ´Â ¿øÀÎ ºÒ¸íÀÇ µå¹® ÁúȯÀ¸·Î¼­, ÁÖ·Î ´ë³ú ¹Ý±¸¸¦ ħ¹üÇϸç, Á¶±â¿¡ Àå´Ô, ±Í¸Ó°Å¸®, °¨°¢Àå¿¡ µîÀÇ Áõ»óÀÌ ³ªÅ¸³­´Ù. 2. ¹éÁú³úÁõÀÇ ¾Æ±Þ¼º ¶Ç´Â ¸¸¼ºÇüÀ¸·Î ¼Ò¾Æ ¹× û³â¿¡°Ô¼­ º¼ ¼ö ÀÖ´Ù. ÀÓ»óÁõ»óÀ¸·Î´Â ½Ç¸í, ³­Ã», ¾çÃø¼º °æ·Ã, ÁøÇ༺ Á¤½ÅȲÆó µîÀÌ ³ªÅ¸³­´Ù. ´ë³ú ¹éÁúÀÇ ±¤¹üÇÑ ÆÄ±«°¡ ÀÖ°í, °øµ¿ÀÌ Çü¼ºµÈ´Ù. º¸Åë »ê¹ßÀûÀ¸·Î ¹ß»ýÇϳª °¡Á·¼ºÀÇ º´ÇüÀ¸·Îµµ º¸°íµÇ¾î ÀÖ´Ù.
  • Schmorl's disease
    ½¬¸ð¸¦ º´
    1. ÀÎÁ¢ÇÑ º¹Ã¼ºÎ¿¡ÀÇ ¼öÇÙ Å»Ãâ.
  • Scholz's disease
    ¼ñÃ÷ º´
    ¹éÁú ³úÁõÀÇ °¡Á· ¼ºÇüÀ¸·Î ¹Ý¼º ¿­¼º À¯Àü. 8¼¼ °æ¿¡ ½ÃÀÛÇÏ¿© ³ú¹éÁúÀÇ Å»¼öÈ­, °¨°¢¼º ½Ç¾îÁõ, ÇÇÁú¼º ½Ç¸í, ³­Ã», Çã¾à, »çÁöÀÇ °æ·Ã, ¿ÏÀü ¸¶ºñ, Ä¡¸Å°¡ Ư¡ÀÌ´Ù.
  • seasonal disease
    °èÀýº´
    °èÀý¿¡ µû¶ó ¹ß»ýÇÏ´Â º´ÀÇ ÃÑĪ. °èÀýÀÇ º¯È­°¡ º´À» ÀÏÀ¸Å²´Ù´Â °ÍÀ» óÀ½ ±â·ÏÇÑ »ç¶÷Àº È÷Æ÷Å©¶óÅ×½º¿´´Âµ¥, À̸¦ ±Ù´ë ÀÇÇÐÀûÀÎ ¹æ¹ýÀ¸·Î ¿¬±¸ÇÑ »ç¶÷Àº µ¶ÀÏÀÇ µ¥ ·ç´õ¿´´Ù. ±×´Â ±â´Ü ±³Ã¼ ¶§ÀÇ Àü¼± Åë°ú¿Í °¢Á¾ Áúº´°úÀÇ °ü·ÃÀ» Åë°èÇÐÀûÀ¸·Î Á¶»çÇÏ¿´À¸¸ç, ƯÈ÷ ºÏ¹Ý±¸ÀÇ °èÀý°ú °ü°è°¡ ±íÀº Áúº´ÀÇ ¿¬°£ºÐÆ÷Ç¥´Â °èÀýº´ ͏°´õÀÇ ½ÃÃʷμ­ À¯¸íÇÏ´Ù. ¾î¶² º´À» °èÀýº´À¸·Î Ãë±ÞÇϱâ À§Çؼ­´Â, ±× º´ÀÇ À¯¹ßÀÎÀÚ ¶Ç´Â ±× º´À» Àü¿°½ÃŰ´Â À§»ý °ïÃæ µîÀÌ °èÀýÀûÀ¸·Î º¯µ¿Çϰí ÀÖ´Ù´Â Á¡, ¶Ç´Â Àΰ£ ÀÚü°¡ ±× º´¿¡ °É¸®±â ½¬¿î »óŰ¡ °èÀý¿¡ ÀÇÇØ¼­ Á¿ìµÈ´Ù´Â Á¡ µîÀÌ ¾î¶»°Ô ¼­·Î ¾ôÇô ÀÖ´ÂÁö Á¶»çÇÒ Çʿ䰡 ÀÖ´Ù. Çѱ¹ÀÇ °æ¿ì, ¾î¸°ÀÌÀÇ ¼ÒÈ­±â º´À̳ª ´Üµ¶ µîÀÇ ÇǺΠÁúȯÀº ¿©¸§¿¡ ¸¹°í, °Ü¿ï¿¡¼­ º½¿¡ À̸£·¯ Â÷°í ¸Þ¸¶¸¥ ±âÈÄÀÏ ¶§¿¡´Â °¨±â, Æó·Å, ±Þ¼º ±â°üÁö¿° µîÀÌ ¸¹´Ù.
  • self limited disease
    ÀÚ±â ÇÑÁ¤¼º Áúȯ
    Áúȯ ÀÚüÀÇ ¼ºÁú ¶§¹®¿¡ ÀÏÁ¤Çϰí ÇÑÁ¤µÈ °æ°í¸¦ ÃëÇÏ´Â Áúȯ.
  • sexually transmitted disease
    ¼º Àü¿°¼º Áúȯ
    Åë»óÀûÀÎ ¼º±³¿¡ ÀÇÇÑ ¼ºº´À» Æ÷ÇÔÇÏ¿©, ¼º±³´Â ¾Æ´ÏÁö¸¸ À¯»çÇÑ ¼º ÇàÀ§·Î °¨¿°µÇ´Â ¸ðµç Áúȯ. ¼º¿¡ ´ëÇÑ »çȸ °ü½ÀÀº Áö³­ ¼ö ½Ê ³â¿¡ °ÉÃÄ ¸¹ÀÌ º¯È­ÇÏ¿´À¸¸ç, 1970³â´ë¿¡ À̸£·¯ ¼º ÇàÀ§ÀÇ ´Ù¾ç¼ºÀÌ µÎµå·¯Áö°Ô ³ªÅ¸³µ´Ù. Áï, À̼º°£ÀÇ ¼º±³»Ó¸¸ ¾Æ´Ï¶ó µ¿¼º°£¿¡ ÇàÇÏ¿©Áö´Â ¿©·¯ ÇüÅÂÀÇ ¼º ÇàÀ§, ¿©·¯ »ó´ëÀÚ¿ÍÀÇ ¼º °ü°è, ´Ù¾çÇÑ ¼º ±â±³ ¹× ±¸°­ ¼º±â ¼º ÇàÀ§ µî ´Ù¾çÇØÁ³À¸¸ç, ÀÌ¿¡ µû¶ó °¨¿°ÀÇ Á¾·ùµµ Áõ°¡ÇÏ¿´´Ù. ¶ÇÇÑ °¨¿° °æ·Îµµ Åë»óÀû ¼º±³ ¿Ü¿¡ ±¸°­ ¹× ¼º±â¿¡ÀÇ ÀÔ¸ÂÃã¿¡ ÀÇÇÑ °æ±¸ °¨¿°, µ¿¼º¾Ö ³²¼º°£¿¡ ÇàÇÏ¿©Áö´Â Ç×¹® ¼º±³ ¹× ¿©·¯ »ç¶÷ÀÌ ¾î¿ï·Á ºÒ°áÇÏ°Ô À̺ÎÀÚ¸®¸¦ °°ÀÌ »ç¿ëÇÏ´Â µ¥¼­ ¿À´Â ±â»ýÃæ °¨¿° µî ¿©·¯ °¡Áö°¡ ÀÖ´Ù. ¼º Àü¿°¼º ÁúȯÀ» ÀÏÀ¸Å°´Â º´¿øÃ¼µµ ´Ù¾çÇÏ¿©, ´ëº°ÇØ º¸¸é, ¼¼±Õ, ¹ÙÀÌ·¯½º, Ŭ¶ó¹Ìµð¾Æ Æ®¶óÄÚ¸¶Æ¼½º
  • silo-filler's disease
    »çÀÏ·Î Ãæ¸¸ °¡½ºº´
    ¶§¶§·Î ±Þ¼º Æó ºÎÁ¾À» ¼ö¹ÝÇÏ´Â ÆóÀÇ ¿°ÁõÀ¸·Î, »çÀϷο¡ ¸ðÀÎ Àڱؼº °¡½ºÀÇ ÈíÀÔÀÌ ¿øÀÎÀÌ´Ù.
  • Simmonds' disease
    ½Ã¸óµå º´, ½Ã¸óÁ
    1. ÇϼöüÀÇ À§ÃàÀ¸·Î ÀÎÇØ ±ØµµÀÇ ¼è¾à, ¼Ò¸ð, ¹× Á¤½Å Àå¾Ö¸¦ À¯¹ßÇϰí, Á¶·Î, Å»¸ð, ¼º¿å °¨Åð, ±âÃÊ ´ë»ç ÀúÇÏ µîÀ» Ư¡À¸·Î Çϴµ¥ ÁÖ·Î ¿©ÀÚ¿¡¼­ º¼ ¼ö ÀÖ´Ù. 2. somatotro
  • smith strang disease : ¸ÞŸÀÌ¿À´Ñ Èí¼ö Àå¾Ö¿¡ ÀÇÇÑ °ÍÀ¸·Î »ó¿°»öü¼º ¿­¼º ÇüÁú·Î À¯ÀüµÈ´Ù. È© °ÇÁ¶¼Ò³»ÀÇ ³¿»õ¿Í ºñ½ÁÇÑ Æ¯À¯ÇÑ ³¿»õ¸¦ ³»¸ç, À̰ÍÀº Èí¼öµÇÁö ¾ÊÀº ¸ÞŸÀÌ¿À´Ñ¿¡ ´ëÇÑ ¼¼±ÕÀÇ ÀÛ¿ë¿¡ ÀÇÇÏ¿© Á¶¼ºµÇ´Â ¾ËÆÄ ÇÏÀ̵å·Ï½Ã ³«»êÀÌ ¿øÀÎÀÌ´Ù.

    Smith's dis

    ½º¹Ì½º º´
  • Soederland's disease
    Á¦µ¥¸¦¶õµå º´
    »ïÃ⼺ ¹æ±¤¿°À» ¸»Çϴµ¥, ¹«±Õ ³ó´¢º´À̶ó°íµµ ÇÑ´Ù.
  • spirochetal disease
    ½ºÇÇ·ÎÇìŸ Áúȯ
  • sporadic disease
    »ê¹ß Áúȯ, »ê¹ß¼º Áúȯ
  • sterility disease
    ºÒÀÓ¼º Áúȯ
  • Still's disease
    ½ºÆ¿ Áúȯ, ½ºÆ¿ º´
    µ¿ÀǾî=juvenile rheumatoid arthritis. 1. Ç÷û¿¡ ÀÌ»óÀÌ ³ªÅ¸³ªÁö ¾Ê´Â °üÀý¿°À¸·Î¼­ Á¾Á¾ ¹ß¿­°ú ¸²ÇÁÀýº´ÁõÀÌ µ¿¹ÝµÇ¸ç 16¼¼ ÀÌÀü¿¡ ½ÃÀÛÇÏ´Â °üÀý¿°ÀÇ 70%¸¦ Â÷ÁöÇÑ´Ù. 2. ¼Ò¾Æ¼º ¸²ÇÁÁ¾ ºñÁ¾¼º À§Ãà ´Ù¹ß¼º °üÀý¿°. ¼Ò¾Æ¿¡ »ý±â´Â ¸¸¼º ´Ù¹ß¼º °üÀý¿°ÀÇ ÀÏÁ¾. ¸²ÇÁÀý Á¾Ã¢, ºñÁ¾, ºÒ±ÔÄ¢¼º ¹ß¿­ÀÌ Æ¯Â¡ÀÌ´Ù.
  • storage pool disease
    ÀúÀåÁ¶º´
    ÀÀÁýÁ¦, ¿¡Çdz×ÇÁ¸°, ¿ÜÀμº ADP, Æ®·Òºó µî¿¡ ¹ÝÀÀÇÏ¿© ADP¸¦ ¹æÃâÇÏ´Â Ç÷¼ÒÆÇ ±â´É ºÎÀü¿¡ ÀÇÇÑ Ç÷¾× ÀÀ°í Àå¾Ö, °¡º­¿î ÃâÇ÷ Áõ»ó, ÃâÇ÷ ½Ã°£ Áö¿¬, ±³¿øÁúÀ̳ª Æ®·Òºó¿¡ ´ëÇÑ ÀÀÁý ¹ÝÀÀÀÇ °¨Å𸦠Ư¡À¸·Î ÇÑ´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
Marie-Strumpell disease <rheumatology> A polyarthritis involving the spine, which is characterised by progressive, painful stiffening of the joints and ligaments. It almost exclusively affects young men.
Interestingly the disease seems to be associated with HLA B27, those with this histocompatability antigen are 300 times more likely to get the disease, 90% of sufferers have HLA B27
(18 Nov 1997)
Marion's disease A congenital obstruction of the posterior urethra.
(05 Mar 2000)
Recklinghausen's disease of bone Rarefying osteitis with fibrous degeneration and formation of cysts, and with the presence of fibrous nodules on the affected bones. It is due to marked osteoclastic activity secondary to hyperfunction of the parathyroid glands.
(12 Dec 1998)
Recklinghausen's disease type I type 2 neurofibromatosis
Gerhardt-Mitchell disease Disease marked by paroxysmal, bilateral vasodilatation, particularly of the extremities, with burning pain, and increased skin temperature and redness.
(12 Dec 1998)
Gerhardt's disease Disease marked by paroxysmal, bilateral vasodilatation, particularly of the extremities, with burning pain, and increased skin temperature and redness.
(12 Dec 1998)
vertebral-basilar artery disease <cardiology> Aortic arch syndrome, also referred to by many as vertebral-basilar artery disease, carotid artery occlusive syndrome and subclavian steal syndrome is characterised by a constellation of signs and symptoms which occur secondary to abnormalities in the major arteries which extend off of the aortic arch.
These abnormalities are structural and most often secondary to the effects of atherosclerosis, blood clots, trauma or a congenital abnormality. Symptoms of this condition include various neurologic symptoms, reduction in pulse and changes in blood pressure.
(27 Sep 1997)
Gerlier's disease A paroxysmal attack of severe vertigo, not accompanied by deafness or tinnitus, which affects young to middle-aged adults, often following a non-specific upper respiratory infection; due to unilateral vestibular dysfunction.
Synonym: endemic paralytic vertigo, epidemic vertigo, Gerlier's disease, kubisagari, kubisagaru, paralyzing vertigo.
(05 Mar 2000)
Martin's disease A periosteoarthritis of the foot from excessive walking.
(05 Mar 2000)
Carrington's disease <radiology> Idiopathic, associated with allergies and desensitization, variant of Loeffler pneumonia, treatment: corticosteroids Findings: reverse pulmonary oedema pattern (= Loeffler's), areas of consolidation persists (days to weeks) see: eosinophilic lung disease
(12 Dec 1998)
Carrion's disease A generalised, acute, febrile, endemic, and systemic form of bartonellosis; marked by high fever, rheumatic pains, progressive, severe anaemia, and albuminuria.
Synonym: Carrion's disease.
(05 Mar 2000)
gestational trophoblastic disease (choriocarcinoma, molar pregnancy) a type of cancer associated with pregnancy in which a grape-like mole develops in the womb instead of a foetus.
(16 Dec 1997)
parkinson disease Progressive, degenerative disease of unknown aetiology characterised by rhythmic tremor of the limbs, stooped posture, slowness of voluntary movements, and masklike facial expression. Pathologically there is nerve cell loss in the melanin-containing cells in the brainstem and a corresponding reduction in dopamine levels in the corpus striatum. Lewy bodies are present in the substantia nigra and locus coeruleus.
(12 Dec 1998)
parkinson disease, postencephalitic A form of parkinson disease due to degeneration of the corpus striatum or substantia nigra, frequently occurring as a sequel of lethargic encephalitis. The early age of onset, the rapid progression of symptoms and signs of stabilization, and the presence of a variety of other neurological disorders (sociopathic behaviour, tics, spasms, oculogyric crises and other restricted motor disorders, breathing arrhythmias, hyperphagia, and bizarre movements, postures, and gaits) distinguish this disease from the one described by parkinson.
(12 Dec 1998)
parkinson disease, symptomatic Symptoms of parkinson disease induced by drugs, or following cerebral arteriosclerosis, brain tumour, or other central nervous system disorders except encephalitis, which is parkinson disease, postencephalitic.
(12 Dec 1998)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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    ±¸ºÐ/º¸Çè±Þ¿©
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    ÇѱÛ
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    ÇѱÛ
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    ÇѱÛ
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