Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.
KMID : 0391519960030020189
Journal of the Korean Child Neurology Society
1996 Volume.3 No. 2 p.189 ~ p.193
A Case of Joubert Syndrome Confirmed by Ventriculography


Abstract
Joubert syndrome is characterized by episodic hyperpnea, abnormal eye movements, ataxia and mental retardation. It is known to be inherited as an autosomal recessive trait and is more common in the offsprings of consanguineous relationships with
definite preference for the male sex.
KEYWORD
FullTexts / Linksout information
Listed journal information
ÇмúÁøÈïÀç´Ü(KCI) KoreaMed ´ëÇÑÀÇÇÐȸ ȸ¿ø