Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

Familial hypophosphatemia ȯ¾ÆÀÇ Áõ·Êº¸°í

FAMILIAL HYPOPHOSPHATEMIA A CASE REPORT

´ëÇѼҾÆÄ¡°úÇÐȸÁö 2006³â 33±Ç 1È£ p.116 ~ 121
Á¶À±Á¤, ±èÀºÁ¤, ±èÇöÁ¤, ±è¿µÁø, ³²¼øÇö,
¼Ò¼Ó »ó¼¼Á¤º¸
Á¶À±Á¤ ( Cho Yun-Jung ) - °æºÏ´ëÇб³ Ä¡°ú´ëÇÐ ¼Ò¾ÆÄ¡°úÇб³½Ç
±èÀºÁ¤ ( Kim Eun-Jung ) - °æºÏ´ëÇб³ Ä¡°ú´ëÇÐ ¼Ò¾ÆÄ¡°úÇб³½Ç
±èÇöÁ¤ ( Kim Hyun-Jung ) - °æºÏ´ëÇб³ Ä¡°ú´ëÇÐ ¼Ò¾ÆÄ¡°úÇб³½Ç
±è¿µÁø ( Kim Young-Jin ) - °æºÏ´ëÇб³ Ä¡°ú´ëÇÐ ¼Ò¾ÆÄ¡°úÇб³½Ç
³²¼øÇö ( Nam Soon-Hyeun ) - °æºÏ´ëÇб³ Ä¡°ú´ëÇÐ ¼Ò¾ÆÄ¡°úÇб³½Ç

Abstract

°¡Á·¼º ÀúÀλêÇ÷Áõ(famiial hypophosphatemia)Àº ±ÙÀ§ ¼¼´¢°üÀÇ Àλê ÀçÈí¼ö ±âÀüÀÇ °áÇÌÀ¸·Î Ç÷û Ä®½· ³óµµ´Â Á¤»óÀ̳ª Ç÷û ÀÎ»ê ³óµµ°¡ ³·¾ÆÁ® ÀúÀλêÇ÷ÁõÀ» ³ªÅ¸³»´Â °¡Àå ÈçÇÑ À¯Àü¼º ±¸·çº´ÀÌ´Ù. Ç÷û ÀλêÀÌ ³·À½¿¡µµ ºÒ±¸ÇÏ°í, ¼Òº¯À¸·ÎÀÇ ÀÎ»ê ¹èÃâÀÌ Áõ°¡µÇ¾î ÀÖ°í Ç÷û ¾ËÄ®¸®¼º ÀÎ»ê ºÐÇØ È¿¼ÒÀÇ »ó½ÂÀÌ ÇöÀúÇÏ´Ù. ÁÖ·Î ¹Ý¼º ¿ì¼º À¯ÀüÀÌ¸ç º¸Åë ³²¾Æ¿¡¼­ ¿©¾Æº¸´Ù ÀÓ»ó Áõ»óÀÌ ½ÉÇÏ´Ù.

ÀÌ·¯ÇÑ °¡Á·¼º ÀúÀλêÇ÷Áõ ȯÀÚÀÇ Àü½ÅÀû ¼Ò°ßÀ¸·Î´Â ¾ÕÀ̸¶ÀÇ µ¹Ãâ, »ç°¢Çü ¸Ó¸®, ÀÛÀº Å°, ÈØ ´Ù¸®°¡ ³ªÅ¸³ª¸ç, Ä¡°úÀû ¼Ò°ßÀ¸·Î Ä¡Á¶¹é¼±°ú Ä¡³¶ÀÇ ºñ¹Ú, ¾ãÀº ¹ý¶ûÁú, È®ÀåµÈ Ä¡¼ö°­°ú ±Ù°ü, Ä¡±Ù´Ü ³ó¾ç°ú Ä¡ÁÖ ³ó¾çÀÇ ³ôÀº ¹ß»ý·ü, ¿øÀκҸíÀÇ Ä¡±Ù´Ü Èñ¹ÚÈ­ °ñ¿°ÀÌ ³ªÅ¸³­´Ù.

º» Áõ·Ê´Â À¯Ä¡ ÃæÄ¡ Ä¡·á¸¦ À§ÇØ ³»¿øÇÑ È¯¾Æ°¡ ÀÓ»óÀûÀ¸·Î ÀÛÀº Å°¿Í ÈØ ´Ù¸®, ¹æ»ç¼±ÀûÀ¸·Î ¸¹ÀÌ È®ÀåµÈ Ä¡¼ö°­°ú ±Ù°üÀÌ °üÂûµÇ¾î ¼Ò¾Æ°ú¿¡ ÀÇ·ÚÇÑ ¹Ù °¡Á·¼º ÀúÀλêÇ÷ÁõÀ¸·Î Áø´Ü¹Þ¾Æ ±× ÀÓ»óÀû ¼Ò°ß°ú Ä¡°úÀû Ä¡·á¿¡ ´ëÇØ º¸°íÇÏ´Â ¹ÙÀÌ´Ù.

Familial hypophosphatemia is the most common hereditary rickets which occur hypophosphatemia as the calcium concentration in the blood serum is normal but the phosphate concentration in the blood serum decreases by dysfunction of renaltubular phosphorus reabsorption. In spite of the low concentration of phosphate in the blood serum discharge of phosphate by urine and alkaline phosphatase increases remarkably. It is a sex-linked and normally male show severe clinical symptoms than female.

This kind of familial hypophosphatemia patients show frontal bossing. square head, short of status for general finding, and for dental finding, thinning of limina dura and dental follicle, thin and hypoplastic enamel, enlarged pulp chamber and canal, high occurance rate of periapical and periodontal abscess and unknown cause of rarefying osteitis.

This case is to report about the clinical finging and dental treatment of a child patient, who came to the hospital for treatment of deciduous teeth caries but was refered to pediatrics because the child showed clinically short of status, bow-leg and radiographically enlarged pulp chamber and canal, there as diagnosed as familial hypophosphatemia.

Å°¿öµå

°¡Á·¼º ÀúÀλêÇ÷Áõ;Ä¡±Ù´Ü ³ó¾ç
Familial hypophosphatemia;Periapical abscess

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

 

µîÀçÀú³Î Á¤º¸

KCI