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A Case of Nonsyndromic Intrahepatic Bile Duct Paucity with Congenital Bilateral Vocal Cord Paralysis and 13q Deletion
Á¤ÁÖ¿µ, ÀÌÁ¤¼ö, ±èº´ÀÇ, ÃÖ¸íÀç, ¹Úµ¿Ã¶, ±è»ó¿ì, °°æÈÆ,
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Á¤ÁÖ¿µ ( Chung Ju-Young )
ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
ÀÌÁ¤¼ö ( Lee Jeong-Soo )
ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
±èº´ÀÇ ( Kim Byung-Eui )
ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
ÃÖ¸íÀç ( Chey Myoung-Jae )
ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
¹Úµ¿Ã¶ ( Park Dong-Churl )
ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
±è»ó¿ì ( Kim Sang-Woo )
ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
°°æÈÆ ( Kang Gyeong-Hoon )
¼¿ï´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
KMID : 0816120010040010108
Abstract
Nonsyndromic intrahepatic bile duct paucity is known to be associated with several kinds of etiology such as infection, chromosomal anomaly, metabolic disease and idiopathic. We report a rare case of intrahepatic bile duct paucity with congenital bilateral vocal cord paralysis and 13q deletion.
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Intrahepatic bile duct paucity;13q deletion; Vocal cord paralysis
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