What does friedreich ataxia mean?

Definitions for friedreich ataxia
friedre·ich atax·i·a

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U.S. National Library of Medicine

  1. Friedreich Ataxia

    An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75)

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Numerology

  1. Chaldean Numerology

    The numerical value of friedreich ataxia in Chaldean Numerology is: 4

  2. Pythagorean Numerology

    The numerical value of friedreich ataxia in Pythagorean Numerology is: 6

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"friedreich ataxia." Definitions.net. STANDS4 LLC, 2024. Web. 10 May 2024. <https://www.definitions.net/definition/friedreich+ataxia>.

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