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Published on: July 14, 2016
Familial Behr syndrome-like phenotype with autosomal dominant inheritance
Andre C Felicio1, Clecio Godeiro-Junior, Lucianna G Alberto
1Department of Neurology and Neurosurgery, Federal University of São Paulo, São Paulo, Brazil. cf.andre@gmail.com
Abstract:
Behr syndrome is an autosomal recessive disease characterized by early-onset ataxia, optic atrophy and other signs such as pyramidal tract dysfunction. Autosomal dominant inheritance has also been described. In this case report we present a family pedigree of patients with an inherited autosomal dominant Behr syndrome-like phenotype emphasizing their clinical and neuroimaging features.
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