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  • Title: Familial Behr syndrome-like phenotype with autosomal dominant inheritance.
    Author: Felicio AC, Godeiro-Junior C, Alberto LG, Pinto AP, Sallum JM, Teive HG, Barsottini OG.
    Journal: Parkinsonism Relat Disord; 2008; 14(4):370-2. PubMed ID: 17977780.
    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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