Á¤ºÎÀÇ <4´ë ÁßÁõÁúȯ º¸Àå°È>¿¡ µû¶ó ¿À´Â 3¿ùºÎÅÍ ±ØÈñ±ÍÁúȯ°ú »ó¼¼ºÒ¸í Èñ±ÍÁúȯÀÚÀÇ Èñ±ÍÁúȯ »êÁ¤Æ¯·Ê ÇýÅÃÀÌ °¡´ÉÇØÁ³´Ù.
º¸°Çº¹ÁöºÎ´Â 25ÀÏ, Èñ±ÍÁúȯ »êÁ¤Æ¯·Ê È®´ë¸¦ À§ÇØ ²ÙÁØÈ÷ Èñ±ÍÁúȯ ¶Ç´Â À¯ÀüÀÚ Å¬¸®´ÐÀ» ¿î¿µÇØ¿Â »ó±ÞÁ¾ÇÕº´¿ø 13°³ ±â°üÀ» µî·Ï ±â°üÀ¸·Î ½ÂÀÎÇÏ°í, Áúº´ Äڵ尡 ¾ø°í, µ¿¹ÝµÈ À¯»ç ÁúȯÀ¸·Îµµ Ư·Ê¸¦ ÀÎÁ¤¹Þ±â ¾î·Á¿î ÁúȯÀ» 1Â÷·Î °ËÅäÇÏ¿© 44°³ ±ØÈñ±ÍÁúȯ¿¡ ´ëÇØ ¿ì¼± ÇýÅÃÀ» ºÎ¿©Çϱâ·Î Çß´Ù°í ¹àÇû´Ù.
Èñ±ÍÁúȯ »êÁ¤Æ¯·Ê Á¦µµ´Â °íºñ¿ëÀÌ ¹ß»ýÇÏ´Â Èñ±ÍÁúȯÀÚÀÇ ÀÇ·áºñ ºÎ´ãÀ» ³·Ãß±â À§ÇØ °Ç°º¸Çè¿¡¼ ȯÀÚ º»ÀÎÀÌ ºÎ´ãÇÏ´Â ºñ¿ëÀ» 10%·Î ³·ÃçÁÖ´Â Á¦µµ·Î½á, Áö±Ý±îÁö´Â ºñ±³Àû Áø´Ü±âÁØÀÌ ¸íÈ®ÇÑ 151Á¾ÀÇ Èñ±ÍÁúȯ(´©Àûµî·ÏÀÚ 103¸¸¸í)¿¡ ´ëÇؼ¸¸ Àû¿ëµÇ¾î¿Ô´Ù.
ÀÌ¿¡, ½ÂÀÎ ÀÇ·á±â°üÀº °¡Å縯´ë¼¿ï¼º¸ðº´¿ø, °í·Á´ëÇб³ÀÇ°ú´ëÇкμӱ¸·Îº´¿ø, »ï¼º¼¿ïº´¿ø, ¼¿ï´ëÇб³º´¿ø, ÇѾç´ëÇб³º´¿ø, ¼¿ï¾Æ»êº´¿ø, ¼øõÇâ´ëÇб³ ºÎõº´¿ø, ¾ÆÁÖ´ëÇб³º´¿ø, ¾ç»êºÎ»ê´ëÇб³º´¿ø, ÀÎÁ¦´ëÇб³ ºÎ»ê¹éº´¿ø, °æºÏ´ëÇб³º´¿ø, ´ë±¸°¡Å縯´ëÇб³º´¿ø, Ãæ³²´ëÇб³º´¿ø µîÀ̸ç Ư·Ê ´ë»óÀÌ µÇ´Â ȯÀÚ´Â ½ÂÀÎ ÀÇ·á±â°üÀÇ µî·Ï ´ã´çÀÇ»çÀÇ Áø·á¸¦ ¹Þ°í µî·Ï ½ÅûÀ» ÇÒ ¼ö ÀÖ´Ù.
¿¬¹ø
|
Áúȯ¸í
|
¿µ¹®¸í
|
1
|
¾Ë½ºÆ®·Ò ÁõÈıº
|
Alstrom Syndrome
|
2
|
ARCÁõÈıº
|
ARC syndrom
|
3
|
Cowden ÁõÈıº
|
Cowden syndrome
|
4
|
Dent Áúȯ
|
Dent diseases
|
5
|
GLUT1°áÇÌÁõ
|
Glucose transporter type1(GLUT1) deficiency
|
6
|
KID ÁõÈıº
|
KID(Keratitis-ichthyosis-deafness) syndrome
|
7
|
°¡ºÎÅ° ÁõÈıº
|
Kabuki syndrome
|
8
|
°Á÷Àΰ£ÁõÈıº
|
Stiff-man syndrome(Moersch-Woltman syndrome)
|
9
|
°íÇÔ-½ºÅ¸¿ìÆ®º´
|
Gorham-Stout disease(GSD)
|
10
|
±¼ÁöÇü¼ºÀÌ»ó
|
Campomelic dysplasia
|
11
|
´Ù¹ß¼º °ñ´Ü Çü¼ºÀÌ»ó
|
Multiple epiphyseal dysplasia, MED
|
12
|
´Ü¼ø¼º Ç¥ÇÇ ¼öÆ÷Áõ
|
Epidermolysis bullosa simplex, EBS
|
13
|
µ¥´Ï½º-µå·¡½¬ ÁõÈıº
|
Denys-Drash syndrome
|
14
|
µÎ°³°ñ°£´ÜÇü¼ººÎÀüÁõ
|
Craniometaphyseal dysplasia
|
15
|
¶ó½º¹«¼¾³ú¿°
|
Rasmussen's encephalitis
|
16
|
¶û°Å ±âµå¿Â ÁõÈıº
|
Langer-Giedion syndrome
|
17
|
¹Ð·¯-µðÄ¿ ÁõÈıº
|
Miller-Dieker syndrome
|
18
|
¹Ù¸£µ§ºÎ¸£Å© ÁõÈıº
|
Waardenburg syndrome
|
19
|
¼±Ãµ¼º ¹«°ÅÇÙ±¸¼º Ç÷¼ÒÆÇ°¨¼ÒÁõ
|
Congenital amegakaryocytic thrombocytopenia
|
20
|
¾Ë¶óÁú ÁõÈıº
|
Alagille syndrome
|
21
|
¾Ë·º»ê´õº´
|
Alexander disease
|
22
|
¾ØƲ¸®-ºò½½·¯ÁõÈıº
|
Antley-Bixler syndrome
|
23
|
¾î¸°¼±(¼±Ãµ¼º ºñ´ÃÁõ)
|
Congenital Ichthyosis
|
24
|
¿¡µåÇÏÀÓ-ü½ºÅͺ´
|
Erdheim-Chester disease
|
25
|
À帲ÇÁ°üÈ®ÀåÁõ
|
Intestinal lymphangiectasia
|
26
|
ÁÖ¹öÆ® ÁõÈıº
|
Joubert syndrome
|
27
|
ÁöÅÚ¸¸ ÁõÈıº
|
Gitelman Syndrome
|
28
|
Ä«³ª¹Ýº´
|
Canavan disease
|
29
|
Ä«´Ù½Ç
|
Cadasil
|
30
|
Å¥¶ó¸®³ë ÁõÈıº
|
Currarino syndrome
|
31
|
Å©·ÐÄ«À̵å Ä«³ª´Ù ÁõÈıº
|
Cronkhite-Canada syndrome, CCS
|
32
|
ÅÍÇÁÆÃÀåÁõ
|
tufting enteropathy(interstinal epithelial dyspalsia)
|
33
|
Æи®-·Ò¹ö±×º´
|
Parry-Romberg disease
(Progressive hemifacial atrophy)
|
34
|
Ç¥Çǹڸ®°¢È°ú´ÙÁõ
(¼±Ãµ¼º ¼öÆ÷¼º ºñ´Ã¸ð¾çÈ«»öÇǺÎÁõ)
|
Epidermolytic hyperkeratosis
(congenital bullous ichthyosiform erythroderma)
|
35
|
ÇÁ·¹ÀÌÀú ÁõÈıº
|
Fraser syndrome
|
36
|
ÇìÀÌ-À£½ºÁõÈıº
|
Hay-Wells syndrome
(Ankyloblepharon-ectodermal defects)
|
37
|
¾Ë¶õÇåµçÁõÈıº
|
Allan-Herndon-Dudley syndrome(AHDS)
|
38
|
ÀªÇÁ-Ç㽬ȣ¸¥ÁõÈıº
|
Wolf-Hirschhorn syndrome
|
39
|
ÆÓ¸®½º ÅÍ-ų¸®¾ð ÁõÈıº
|
Pallister - killian syndrome
|
40
|
ÄÚÇîÁõÈıº
|
Cohen Syndrome
|
41
|
ÁøÇ༺ °¡Á·¼º °£³» ´ãÁóÁ¤Ã¼Áõ
|
Progressive familial intrahepatic cholestasis
|
42
|
½´¹ÙÅ©¸¸ÁõÈıº
|
Schwachman-Diamond syndrome
|
43
|
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
|
Adult-onset leukoencephalopathy
with axonal spheroids and pigmented glia
|
44
|
¼±Ãµ¼º °íÀν¶¸°Ç÷Áõ
|
Congenital hyperinsulinaemia
|
[±¸Çý¼± ±âÀÚ]
< ÀúÀÛ±ÇÀÚ © Çì¸ðÇʸ®¾Æ ¶óÀÌÇÁ ¹«´ÜÀüÀç ¹× Àç¹èÆ÷±ÝÁö > |