
pmid: 19129991
Joubert syndrome is a very rare autosomal recessive disorder with only 200 cases reported worldwide.Here we report 4 cases of this rare disorder with MRI findings.
Male, Developmental Disabilities, Infant, Chromosome Disorders, Syndrome, Respiration Disorders, Magnetic Resonance Imaging, Cerebellum, Child, Preschool, Intellectual Disability, Oculomotor Nerve Diseases, Humans, Muscle Hypotonia, Ataxia
Male, Developmental Disabilities, Infant, Chromosome Disorders, Syndrome, Respiration Disorders, Magnetic Resonance Imaging, Cerebellum, Child, Preschool, Intellectual Disability, Oculomotor Nerve Diseases, Humans, Muscle Hypotonia, Ataxia
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