Literature DB >> 17977780

Familial Behr syndrome-like phenotype with autosomal dominant inheritance.

Andre C Felicio1, Clecio Godeiro-Junior, Lucianna G Alberto, Aline P M Pinto, Juliana M F Sallum, Helio G Teive, Orlando G P Barsottini.   

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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Year:  2007        PMID: 17977780     DOI: 10.1016/j.parkreldis.2007.08.008

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  2 in total

1.  Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report.

Authors:  Ting Zeng; Linyan Liao; Yi Guo; Xuxu Liu; Xiaobo Xiong; Yu Zhang; Shi Cen; Honghui Li; Shuzhang Wei
Journal:  BMC Pediatr       Date:  2020-09-03       Impact factor: 2.125

2.  Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene.

Authors:  Angela Pyle; Venkateswaran Ramesh; Marina Bartsakoulia; Veronika Boczonadi; Aurora Gomez-Duran; Agnes Herczegfalvi; Emma L Blakely; Tania Smertenko; Jennifer Duff; Gail Eglon; David Moore; Patrick Yu-Wai-Man; Konstantinos Douroudis; Mauro Santibanez-Koref; Helen Griffin; Hanns Lochmüller; Veronika Karcagi; Robert W Taylor; Patrick F Chinnery; Rita Horvath
Journal:  J Neuromuscul Dis       Date:  2014
  2 in total

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