- autosomal recessive trinucleotide repeat disorder (GAA repeat)
- most common form of hereditary ataxia
- mutation in gene encoding protein frataxin on chromosome 9
- presents with progressive ataxia, cerebellar dysfunction, pyramidal weakness and sensory motor neuropathy
- other features: pes cavus, optic atrophy, hypertrophic cardiomyopathy (50-70% patients)
2 comments:
I would like to thank Ultimate Life Clinic for reversing my father's Amyotrophic Lateral Sclerosis (ALS). My father’s ALS condition was fast deteriorating before he started on the ALS Herbal medicine treatment from Ultimate Life Clinic. He was on the treatment for just 6 months and we never thought my father will recover so soon. He has gained some weight in the past months and he is able to walk with no support. You can reach them through there website www.ultimatelifeclinic.com
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