Joubert Syndrome - A Case Report
Joubert syndrome is a very rare malformation.It is estimated to affect between 1 in 80,000and 1 in 100,000 newborns.Joubert syndromeis an autosomal recessive disorder marked byagenesis of cerebellar vermis, ataxia, hypoto-nia, oculomotor apraxia, neonatal breathingproblems and mental retardation.
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Krishna Institute of Medical Sciences University
2013-07-01
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| Series: | Journal of Krishna Institute of Medical Sciences University |
| Subjects: | |
| Online Access: | http://www.jkimsu.com/jkimsu-vol2no2/jkimsu%20vol%202%20no%202%20july%20-%20dec%202013%20138-140.pdf |