KMID : 0391519960030020189
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Journal of the Korean Child Neurology Society 1996 Volume.3 No. 2 p.189 ~ p.193
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A Case of Joubert Syndrome Confirmed by Ventriculography
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Abstract
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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.
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KEYWORD
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