نتایج جستجو برای: hereditary ataxia

تعداد نتایج: 100227  

Journal: :The neurologist 2001
J A Gosalakkal

BACKGROUND This review examines the causes of ataxias in children. It is a relatively common manifestation of neurological diseases in children. The etiology of ataxia covers a broad range, from infections to rare hereditary metabolic diseases. A systematic approach is required to make the correct diagnosis. REVIEW SUMMARY The more common causes of ataxias in children are discussed in detail....

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2008
Robert D Wells

Friedreich ataxia, the most common inherited ataxia, is caused by the transcriptional silencing of the FXN gene, which codes for the 210 amino acid frataxin, a mitochondrial protein involved in iron-sulfur cluster biosynthesis. The expansion of the GAA x TTC tract in intron 1 to as many as 1700 repeats elicits the transcriptional silencing by the formation of non-B DNA structures (triplexes or ...

Journal: :The Journal of Nervous and Mental Disease 1898

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 1980

Ali Fasihi Maryam Godarziyan Morteza Hashemzadeh-Chaleshtori Shahin Ramazi

Background & Aims: Nearly 30 hereditary disorders in humans result from an increase in the number of copies of simple repeats in genomic DNA, including fragile X syndrome, myotonic dystrophy, Huntington’s disease, and Friedreich’s ataxia. One the most frequently occurring types of mutation is trinucleotide repeat expansion. The present study was conducted with the aim of investigating the cause...

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