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A Case of Neonatal Onset Joubert Syndrome

Lee G, Kim EY, Sun KG, Na KH, Park SY, Kim KS, Kim YW

  • KMID: 2099081
  • J Korean Soc Neonatol.
  • 2004 Nov;11(2):230-235.
Joubert syndrome is a rare autosomal recessive disorder characterized by cerebellar vermian hypoplasia, hypotonia, developmental delay, abnormal respiratory patterns and abnormal eye movements. It is usually diagnosed during infancy or...
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