"Friedreich Ataxia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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)
Descriptor ID |
D005621
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MeSH Number(s) |
C10.228.140.252.700.150 C10.228.854.787.200 C10.574.500.825.200 C16.320.400.780.200 C18.452.660.300
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Concept/Terms |
Friedreich Ataxia- Friedreich Ataxia
- Ataxia, Friedreich
- Ataxias, Friedreich
- Friedreich Ataxias
- Friedreich Familial Ataxia
- Ataxia, Friedreich Familial
- Familial Ataxia, Friedreich
- Friedreich Hereditary Ataxia
- Ataxia, Friedreich Hereditary
- Hereditary Ataxia, Friedreich
- Friedreich Hereditary Spinal Ataxia
- Friedreich Spinocerebellar Ataxia
- Ataxia, Friedreich Spinocerebellar
- Spinocerebellar Ataxia, Friedreich
- Friedreich's Ataxia
- Ataxia, Friedreich's
- Friedreich's Disease
- Disease, Friedreich's
- Friedreich's Familial Ataxia
- Ataxia, Friedreich's Familial
- Familial Ataxia, Friedreich's
- Friedreichs Familial Ataxia
- Friedreich's Hereditary Ataxia
- Ataxia, Friedreich's Hereditary
- Ataxias, Friedreich's Hereditary
- Friedreich's Hereditary Ataxias
- Friedreichs Hereditary Ataxia
- Hereditary Ataxia, Friedreich's
- Hereditary Ataxias, Friedreich's
- Friedreich's Hereditary Spinal Ataxia
- Hereditary Spinal Ataxia, Friedreich
- Hereditary Spinal Ataxia, Friedreich's
- Hereditary Spinal Sclerosis
- Hereditary Spinal Scleroses
- Scleroses, Hereditary Spinal
- Spinal Scleroses, Hereditary
- Spinal Sclerosis, Hereditary
- Sclerosis, Hereditary Spinal
- Friedreich Disease
- Disease, Friedreich
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Below are MeSH descriptors whose meaning is more general than "Friedreich Ataxia".
Below are MeSH descriptors whose meaning is more specific than "Friedreich Ataxia".
This graph shows the total number of publications written about "Friedreich Ataxia" by people in this website by year, and whether "Friedreich Ataxia" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1994 | 0 | 1 | 1 |
1997 | 1 | 0 | 1 |
1998 | 3 | 0 | 3 |
1999 | 1 | 0 | 1 |
2000 | 0 | 1 | 1 |
2002 | 1 | 0 | 1 |
2003 | 2 | 1 | 3 |
2004 | 2 | 1 | 3 |
2005 | 2 | 2 | 4 |
2006 | 1 | 0 | 1 |
2007 | 2 | 1 | 3 |
2008 | 2 | 0 | 2 |
2010 | 1 | 0 | 1 |
2011 | 1 | 0 | 1 |
2012 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2016 | 3 | 1 | 4 |
2017 | 1 | 0 | 1 |
2019 | 1 | 0 | 1 |
2021 | 2 | 0 | 2 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Friedreich Ataxia" by people in Profiles.
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Double blind trial of a deuterated form of linoleic acid (RT001) in Friedreich ataxia. J Neurol. 2023 Mar; 270(3):1615-1623.
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Blood Neurofilament Light Chain in Genetic Ataxia: A Meta-Analysis. Mov Disord. 2022 01; 37(1):171-181.
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Reverse Phase Protein Array Reveals Correlation of Retinoic Acid Metabolism With Cardiomyopathy in Friedreich's Ataxia. Mol Cell Proteomics. 2021; 20:100094.
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Changes detected in swallowing function in Friedreich ataxia over 12 months. Neuromuscul Disord. 2019 10; 29(10):786-793.
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Double-blind, randomized and controlled trial of EPI-743 in Friedreich's ataxia. Neurodegener Dis Manag. 2018 08; 8(4):233-242.
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Synthetic transcription elongation factors license transcription across repressive chromatin. Science. 2017 12 22; 358(6370):1617-1622.
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Longitudinal gait and balance decline in Friedreich's Ataxia: A pilot study. Gait Posture. 2017 06; 55:25-30.
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Loss of Frataxin activates the iron/sphingolipid/PDK1/Mef2 pathway in mammals. Elife. 2016 11 30; 5.
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Metal Homeostasis Regulators Suppress FRDA Phenotypes in a Drosophila Model of the Disease. PLoS One. 2016; 11(7):e0159209.
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Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegeneration. Elife. 2016 06 25; 5.