Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

±âÀú¼¼Æ÷¸ð¹ÝÁõÈıº°ú ¿¬°üµÈ ´Ù¹ß¼º Ä¡¼º°¢È­³¶Á¾ÀÇ Ä¡Çè 2·Ê

Case Report Of Multiple Odontogenic Keratocysts With Basal Cell Nevus Syndrome

¹ÚÁöÇö, À±±¸È£, Á¤Á¤±Ç, ¹Ú°ü¼ö, ½ÅÀç¸í, ÃÖ¹®°æ,
¼Ò¼Ó »ó¼¼Á¤º¸
¹ÚÁöÇö ( Park Ji-Hyun ) - ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ »ó°è¹éº´¿ø ±¸°­¾Ç¾È¸é¿Ü°ú
À±±¸È£ ( Yoon Kyu-Ho ) - ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ »ó°è¹éº´¿ø ±¸°­¾Ç¾È¸é¿Ü°ú
Á¤Á¤±Ç ( Cheong Jeong-Kwon ) - ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ »ó°è¹éº´¿ø ±¸°­¾Ç¾È¸é¿Ü°ú
¹Ú°ü¼ö ( Park Kwan-Soo ) - ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ »ó°è¹éº´¿ø ±¸°­¾Ç¾È¸é¿Ü°ú
½ÅÀç¸í ( Shin Jae-Myung ) - ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ »ó°è¹éº´¿ø ±¸°­¾Ç¾È¸é¿Ü°ú
ÃÖ¹®°æ ( Choi Mun-Kyung ) - ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ »ó°è¹éº´¿ø ±¸°­¾Ç¾È¸é¿Ü°ú

Abstract


Basal cell nevus syndrome, also known as Gorlin-Goltz syndrome, is a hereditary condition transmitted as an autosomal dominant trait that exhibits high penetrance and variable expressivity. It is an ecto-mesodermal polydysplasia with numerous manifestations that affect multiple organs. Odontogenic keratocysts, palmar and plantar pits, and hypertelorism are the most frequently observed anomalies. Currently there are new lines of investigation based on biomolecular studies, which aim at identifying the molecules responsible for these cysts and thus early allowing an early diagnosis of these patients. We report two cases of multiple odontogenic keratocysts associated with basal cell nevus syndrome.

Å°¿öµå

Odontogenic keratocyst;Basal cell nevus syndrome

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

 

µîÀçÀú³Î Á¤º¸

KCI
KoreaMed