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"familial amyloidosis"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
¿µ¹® amyloidosis ÇÑ±Û ¾Æ¹Ð·ÎÀ̵åÁõ
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  º»·¡ »ýü¿¡´Â ¾ø´Â ´ç´Ü¹éÁúÀÇ ÀÏÁ¾À¸·Î ºñÁ¤»óÀûÀ¸·Î ¾Æ¹Ð·ÎÀ̵å´Ü¹éÀÌ Á¶Á÷À̳ª Àå±â¿¡ Ä§ÂøµÇ´Â º´. ¹ßÇöºÎÀ§°¡ Àü½Å¼ºÀΠ°æ¿ìÀÇ ¾Æ¹Ð·ÎÀ̵åÁõ(Àü½Å¼º ¾Æ¹Ð·ÎÀ̵åÁõ)¿¡´Â ¸í¹éÇÑ ¿øÀξøÀÌ ÀϾ´Â ¿ø¹ß¼º ¾Æ¹Ð·ÎµåÁõ°ú ¸¸¼ºÈ­³ó¼º ¿°ÁõÀ̳ª °áÇÙ µî ¼Ò¸ð¼º Áúȯ¿¡¼­ Ã£¾Æº¼ ¼ö Àִ ¼Ó¹ß¼º ¾Æ¹Ð·ÎÀ̵åÁõÀÌ ÀÖ´Ù. ¹ßÇöºÎÀ§°¡ ±¹¼Ò¼ºÀΠ°æ¿ìÀÇ ±¹¼Ò¼º ¾Æ¹Ð·ÎÀ̵åÁõÀ¸·Î¼­´Â ³úÀÇ ³ëÀιÝÀÌ ±× ¿¹À̸ç, Æ¯È÷ ÀԾȿ¡¼­´Â Çô³ª ÀÕ¸ö¿¡ ´ëÇÑ Ä§ÂøÀÌ ÇöÀúÇÏ°í ¿©·¯ °¡Áö ±â´ÉÀå¾Ö¸¦ ³ªÅ¸³½´Ù. Á¶Á÷ÇÐÀûÀ¸·Î´Â Ç츶Åå½Ç¸° ¿¡¿ÀÁø¿°»ö¿¡¼­´Â ¿¡¿ÀÁø¼º ¹«±¸Á¶ÀΠÀ¯¸®È­¸¦ ³ªÅ¸³»¸ç Äá°í·¹µå, Æí±¤»ó(³ì»ö) µîÀ¸·Î È®ÀÎÇÑ´Ù. ±¸Á¶ÀûÀ¸·Î´Â ¾Æ¹Ð·ÎÀ̵堼¶À¯ÀÇ ÁýÇÕÀ¸·Î ÀÌ·ç¾îÁö´Â ¿©·¯ °¡Áö ¾Æ¹Ð·ÎÀ̵å Ä§ÂøÀÌ ÀÖÀ¸¸ç ±×°Íµé¿¡ ´ëÇÑ º´ÇüÀÌ ºÐ·ùµÇ¾î ÀÖ´Ù. °¡Á·Çü, ´Ù¹ß¼º °ñ¼öÁ¾°ú ¼ö¹ÝÇϴ Çü ±×¸®°í °¡Á·¼º ÁöÁßÇØ¿­À» ¼ö¹ÝÇϴ Çü µîÀÌ ÀÖ´Ù.
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  • ¿µ¹®
    ÇѱÛ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ
  • endocardial amyloidosis
    ½É(Àå)³»¸·¾Æ¹Ð·ÎÀ̵åÁõ
  • generalized amyloidosis
    Àü½Å¾Æ¹Ð·ÎÀ̵åÁõ
  • nodular amyloidosis
    °áÀý¾Æ¹Ð·ÎÀ̵åÁõ
  • primary amyloidosis
    ¿ø¹ß¾Æ¹Ð·ÎÀ̵åÁõ
  • systemic amyloidosis
    Àü½Å¾Æ¹Ð·ÎÀ̵åÁõ
  • senile amyloidosis
    ³ë³â¾Æ¹Ð·ÎÀ̵åÁõ
  • acholuric familial jaundice
    ¹«´ãÁó´¢°¡Á·¼ºÈ²´Þ
  • familial
    °¡Á·(¼º)-
  • familial adenomatous polyposis
    °¡Á·¼º»ùÁ¾Æú¸³Áõ
  • familial aminoglycoside ototoxicity
    °¡Á·¼º¾Æ¹Ì³ë±Û¸®Äڽõå±Íµ¶¼º
  • familial amyloid neuropathy
    °¡Á·¼º¾Æ¹Ð·ÎÀ̵å½Å°æº´(Áõ)
  • familial annulare erythema
    °¡Á·¼ºÀ±»óÈ«¹Ý, °¡Á·¼º°í¸®È«¹Ý
  • familial cardiomyopathy
    °¡Á·¼º½ÉÀå±ÙÀ°º´(Áõ), °¡Á·¼º½É±Ùº´(Áõ)
  • familial dysautonomia
    °¡Á·¼ºÀÚÀ²½Å°æÀÌ»ó(Áõ)
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ
  • familial adenomatous polyposis
    °¡Á·¼ºÅ«Ã¢ÀÚÆú¸³Áõ, °¡Á·¼º´ëÀåÆú¸³Áõ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ
  • endocardial amyloidosis
    ½ÉÀå³»¸·¾Æ¹Ð·ÎÀ̵åÁõ
  • generalized amyloidosis
    Àü½Å¾Æ¹Ð·ÎÀ̵åÁõ
  • nodular amyloidosis
    °áÀý¾Æ¹Ð·ÎÀ̵åÁõ
  • primary amyloidosis
    ¿ø¹ß¾Æ¹Ð·ÎÀ̵åÁõ
  • senile amyloidosis
    ³ëÀξƹзÎÀ̵åÁõ
  • systemic amyloidosis
    Àü½Å¾Æ¹Ð·ÎÀ̵åÁõ
  • acholuric familial jaundice
    (¢¡hereditary spherocytosis) À¯ÀüµÕ±ÙÀûÇ÷±¸Áõ, À¯Àü±¸ÇüÀûÇ÷±¸
  • familial cardiomyopathy
    °¡Á·½ÉÀå±ÙÀ°º´Áõ
  • familial dyskeratotic comedo
    °¡Á·°¢È­ÀÌ»ó¸éÆ÷
  • familial dysautonomia
    °¡Á·ÀÚÀ²½Å°æ±â´ÉÀÌ»ó
  • endogenous familial hypertriglyceridemia
    ³»Àΰ¡Á·°íÁß¼ºÁö¹æÇ÷Áõ
  • familial eosinophilia
    °¡Á·È£»ê±¸Áõ°¡Áõ
  • familial annulare erythema
    °¡Á·À±»óÈ«¹Ý, °¡Á·°í¸®È«¹Ý
  • familial pigmented purpuric eruption
    °¡Á·»ö¼ÒÀڹݹßÁø
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Familial hypercholesterolemia
    °¡Á·¼º(Ê«ðéàõ) °í(ÍÔ)ÄÝ·¹½ºÅ×·ÑÇ÷Áõ(úìñø)
  • Hailey-Hailey disease = familial benign chronic pemphigus
    ÇìÀϸ®-ÇìÀϸ®º´
  • amaurotic familial idiocy =Tay-Sachs disease
    °¡Á·¼ºÈæ¾Ï½Ã¹éÄ¡(Ê«ðéàõýÙÒ®î¡ÛÜöÁ).
  • amaurotic familial idiocy =Tay-Sachs disease
    °¡Á·¼º Èæ³»Àå ¹éÄ¡(Ê«ðéàõýÙÒ®î¡ÛÜöÁ).
  • hearing loss, familial pregressive
    °¡Á· ÁøÇà(¼º) ³­Ã»
  • hyperbilirubinemia,asymptomatric familial
    ¹«ÁõÈÄ °¡Á·¼º(Ùíñøý¦ Ê«ðéàõ)
  • hypercholesterolemia,familial
    °¡Á·¼º(Ê«ðéàõ)
  • idiopathic familial fibromatosis
    Ư¹ß¼º °¡Á·¼º ¼¶À¯Á¾Áõ.
  • idiopathic familial fibromatosis
    Ư¹ß¼º °¡Á·¼º ¼¶À¯Á¾Áõ
  • infantile amaurotic familial idiocy
    ¿µ¾Æ¼º Èæ³»À强 °¡Á·¼º ¹éÄ¡.
  • infantile amaurotic familial idiocy
    ¿µ¾Æ¼º Èæ³»À强 °¡Á·¼º ¹éÄ¡.
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ.
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ(¡­ñø), À¯ÀüºÐÁõ(ëºîþÝÏñø)
  • amyloidosis
    À¯ÀüºÐÁõ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ.
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ(¡­ñø), À¯ÀüºÐÁõ(ëºîþÝÏñø)
  • amyloidosis
    À¯ÀüºÐÁõ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ
  • amyloidosis cutis
    ÇǺξƹзÎÀ̵åÁõ
  • amyloidosis primary
    ¿ø¹ß¼º(ê«Û¡àõ) ¾Æ¹Ð·ÎÀ̵åÁõ.
  • amyloidosis ulcer
    À¯ÀüºÐÁõ(ëºîþÝÏñø) ±Ë¾ç(Ï÷åË)
  • cardiac amyloidosis
    ½É¾Æ¹Ì·ÎÀ̵µÁõ À¯ÀüºÐÁõ(ãý-ñø ëºîþÝÏñø)
  • cutaneous amyloidosis
    ÇǺÎÀ¯ÀüºÐÁõ
  • endocardial amyloidosis
    ½É³»¸·¾Æ¹Ð·ÎÀ̵åÁõ.
  • generalized amyloidosis
    Àü½Å¼º ¾Æ¹Ð·ÎÀ̵åÁõ.
  • hepatic amyloidosis
    °£¾Æ¹Ð·ÎÀ̵åÁõ.
  • hereditary cerebral hemorrhages with amyloidosis(hchwa)
    À¯Àü¼º ³úÃâÇ÷, ¾Æ¹Ð·ÎÀ̵åÁõ¼º
  • localized amyloidosis
    ±¹ÇѼºÀ¯ÀüºÐÁõ
  • macular amyloidosis
    ¹Ý»ó À¯ÀüºÐÁõ
´ëÇѱâ»ýÃæÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • familial aggregation
    °¡Á·ÁýÀû¼º
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ(ñø)
  • familial high-density lipoprotein deficiency °¡Á·¼º °í¹Ðµµ ÁöÁú´Ü¹éÁú °áÇÌ (Ê«ðéàõÍÔÚËÓøò·òõ
    Ó±ÛÜòõÌÀù¹)
  • familial hypercholesterolemia
    °¡Á·¼º(Ê«ðéàõ) °ú(Φ)ÄÝ·¹½ºÅ×·ÑÇ÷Áõ(úìñø)
  • familial lysosomal lipase deficiency
    °¡Á·¼º(Ê«ðéàõ) ¶óÀÌ¼Ò¼Ø ¶óÀÌÆäÀ̽º °áÇÌ(ÌÀù¹)
  • familial methemoglobinemia
    °¡Á·¼º(Ê«ðéàõ) ¸ÞÅ׸ð±Û·ÎºóÇ÷Áõ(úìñø)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 3 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ
  • familial
    °¡Á·¼ºÀÇ
  • familial polyposis
    °¡Á·¼ºÆú¸³Áõ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
AL absolute latency; acinar lumen; acute leukemia; adaptation level; albumin; alcoholism [and other dru...
DAA decompensated autonomous adenoma; dementia associated with alcoholism; dialysis-associated amyloidos...
HCHWA hereditary cerebral hemorrhage with amyloidosis
FHH Familial Hypocalciuric Hypercalcemia
  = Familial Benign Hypercalcemia
FAD familial Alzheimer dementia; familial autonomic dysfunction; fetal activity-acceleration determinati...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
FAF Familial amyloidosis, Finnish type
AL Amyloidosis
DRA Dialysis related amyloidosis
HCHWA-D Hereditary cerebral haemorrhage with amyloidosis, Dutch type
BFNC Benign Familial Neonatal Convulsions
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • endocardial amyloidosis
    ½É³»¸· ¾Æ¹Ð·ÎÀ̵åÁõ
  • hereditary amyloidosis
    À¯Àü¼º À¯ÀüºÐÁõ
    1. À¯Àü¿¡ ÀÇÇØ ¿ø¼¶À¯¼º ´ç ´Ü¹éÀÌ ÇǺÎ, Á¡¸·, ³»ºÎ Àå±â¿¡ ħÀüµÇ´Â º´. 2. À¯ÀüÀûÀ¸·Î ½ÅüÀÇ °¢Á¾ ºÎÀ§¿¡ ¾Æ¹Ð·ÎÀ̵å
  • primary amyloidosis
    ¿ø¹ß¼º À¯ÀüºÐÁõ, ¿ø¹ß ¾Æ¹Ð·ÎÀ̵åÁõ, ¿ø¹ß¼º ¾Æ¹Ð·ÎÀ̵åÁõ
  • amaurotic familial idiocy
    °¡Á·¼º Èæ³»Àå ¹éÄ¡
    µ¿ÀǾî=Tay-Sach's disease.
  • asymptomatric familial hyperbilirubinemia
    ¹«ÁõÈÄ °¡Á·¼º °úºô¸®·çºóÇ÷Áõ
  • benign familial pemphigus
    ¾ç¼º °¡Á·¼º õÆ÷â
    µå¹°°Ô ¹ß»ýÇÏ´Â, À¯Àü¼ºÀ̸ç Áö¼ÓÀûÀ¸·Î Àç¹ßÀ» ¹Ýº¹ÇÏ´Â ¼ÒÆ÷¼º ¹× ÀÛÀº ¼öÆ÷¼º ÇǺο°À¸·Î, ¾×¿Í, ¼­ÇýºÎ ¹× ¸ñ ºÎÀ§¸¦ °¡Àå Àß Ä§¹üÇÏÁö¸¸, ¶§·Î´Â ±¤¹üÇÑ ºÎÀ§¸¦ ħ¹üÇÑ´Ù. º´º¯Àº ´Ù¹ß¼ºÀ̸ç, ¼öÁÖÀÏ ³»Áö ¼ö°³¿ù ÈÄ¿¡ ¼èÅðÇÑ´Ù. ÀÌ ÁúȯÀº »ó¿°»öü ¿ì¼º À¯ÀüÀ» ÇÑ´Ù.
  • familial adenomatous polyposis
    °¡Á·¼º ¼±Á¾¼º ¿ëÁ¾Áõ
  • familial amyloid polyneuropathy
    °¡Á·¼º ¾Æ¹Ð·ÎÀÌµå ´Ù¹ß ½Å°æº´Áõ
  • familial benign chronic pemphigus
    °¡Á·¼º ¾ç¼º ¸¸¼º õÆ÷â
  • familial cold urticaria
    °¡Á·¼º Çѳà µÎµå·¯±â
  • familial cutaneous collagenosis
    °¡Á·¼º ÇǺΠ±³¿øÁõ
  • familial dysbetalipoproteinemia
    °¡Á·¼º ÀÌ»ó º£Å¸ ¸®Æ÷ ÇÁ·ÎÅ×ÀÎ Ç÷Áõ
  • familial fibrous dysplasia
    °¡Á·¼º ¼¶À¯ ÀÌÇü¼º
  • familial genuine malfomation of root
    °¡Á·¼º ¼±Ãµ¼º Ä¡±Ù ±âÇü
    µ¿ÀǾî=dentinal dys
  • familial hemolytic anemia
    °¡Á·¼º ¿ëÇ÷¼º ºóÇ÷
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
familial amyloidosis <neurology> A disorder in which various peripheral nerves are infiltrated with amyloid and their functions disturbed, an abnormal prealbumin is also formed and is present in the blood; characteristically, it begins during mid-life and is found largely in persons of Portuguese descent. Other rare clinical types occur.
Inheritance: autosomal dominant.
Synonym: familial amyloidosis, hereditary amyloidosis.
(05 Mar 2000)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
amyloidosis Deposition of amyloid. A common complication of several diseases (leprosy, tuberculosis), often associated with perturbation of the immune system, although there may be immunosuppression or enhancement.
(18 Nov 1997)
amyloidosis: bone manifestations <radiology> Joint pain without radiographic findings, osteoporosis, especially in axial skeleton, lytic lesions that destroy cortex and invade soft tissue, wrist, scaphoid and lunate lesions that may extend into the carpal tunnel, inducing the classic complaints of carpal tunnel syndrome amyloid arthropathy Differential diagnosis: pigmented villonodular synovitis, synovial chondromatosis, rheumatoid arthritis, TB
(12 Dec 1998)
amyloidosis cutis Localised cutaneous amyloidosis with pruritic brownish-red papules, most commonly on the lower legs, due to amyloid infiltration of the papillary dermis.
Synonym: amyloidosis cutis, lichen amyloidosis.
Origin: G. Leichen, lichen, a lichen-like eruption + eidos, resemblance
(05 Mar 2000)
amyloidosis: gastrointestinal manifestations <radiology> Oesophagus, loss of peristalsis, megaesophagus, stomach, small and rigid (simulate linitis plastica), effaced rugal pattern, diminished/absent peristalsis, may be localised to antrum, amyloidoma: well defined submucosal mass, small bowel, diffuse form (more common), diffuse, uniform thickening of valvulae conniventes, broadened flat undulated mucosal folds (mucosal atrophy), jejunalization of ileum, impaired motility, small bowel dilatation, localised form: multiple small deposits; associated with pseudoobstruction, colon, psudopolyps
(12 Dec 1998)
amyloidosis of multiple myeloma Foci of amyloidosis in mesenchymal tissues of some persons with multiple myeloma; no direct relation between amyloid and Bence Jones protein is conclusively known.
(05 Mar 2000)
macular amyloidosis A localised form of amyloidosis cutis characterised by pruritic symmetrical brown reticulated macules, especially on the upper back; microscopically, amyloid is deposited as small subepidermal globules.
(05 Mar 2000)
renal amyloidosis Renal deposits of amyloid, especially in glomerular capillary walls, which may cause albuminuria and the nephrotic syndrome.
Synonym: amyloid nephrosis.
(05 Mar 2000)
cerebral amyloidosis A condition where there is a deposition of amyloid (insoluble protein) in the walls of the arteries which supply the brain. This results in an increased risk of dementia and-or intracerebral haemorrhage. Cerebral amyloidosis or cerebral amyloid angiopathy, is a complication of primary amyloidosis.
(27 Sep 1997)
primary amyloidosis <immunology, nephrology> A disease which is characterised by the deposition of the fibrous protein amyloid in one or more locations within the body.
Amyloid deposition may occur in the kidney, brain, liver, heart, skin and lungs. A recognised complication is a restrictive cardiomyopathy.
(05 Mar 1998)
hereditary amyloidosis <neurology> A disorder in which various peripheral nerves are infiltrated with amyloid and their functions disturbed, an abnormal prealbumin is also formed and is present in the blood; characteristically, it begins during mid-life and is found largely in persons of Portuguese descent. Other rare clinical types occur.
Inheritance: autosomal dominant.
Synonym: familial amyloidosis, hereditary amyloidosis.
(05 Mar 2000)
secondary amyloidosis Amyloidosis occurring in association with another chronic inflammatory disease; organs chiefly involved are the liver, spleen, and kidneys, and the adrenal glands less frequently.
(05 Mar 2000)
senile amyloidosis A common form of amyloidosis in very old people, usually mild and limited to the heart.
See: amyloidosis of aging.
(05 Mar 2000)
nodular amyloidosis A localised form of amyloidosis in which amyloid occurs as masses or nodules beneath the skin or mucous membranes, e.g., in the larynx.
Synonym: amyloid tumour, focal amyloidosis.
(05 Mar 2000)
focal amyloidosis A localised form of amyloidosis in which amyloid occurs as masses or nodules beneath the skin or mucous membranes, e.g., in the larynx.
Synonym: amyloid tumour, focal amyloidosis.
(05 Mar 2000)
lichen amyloidosis Localised cutaneous amyloidosis with pruritic brownish-red papules, most commonly on the lower legs, due to amyloid infiltration of the papillary dermis.
Synonym: amyloidosis cutis, lichen amyloidosis.
Origin: G. Leichen, lichen, a lichen-like eruption + eidos, resemblance
(05 Mar 2000)
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • familial
    °¡Á·ÀÇ;°¡Á·¼ºÀÇ;°¡Á· ƯÀ¯ÀÇ
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
KMLE ¾àǰ/ÀǾàǰ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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  • ¿µ¹®
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  • ¿µ¹®
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