Friedreich's ataxia risk factors: Difference between revisions
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Aditya Ganti (talk | contribs) (Created page with "__NOTOC__ {{Friedreich's ataxia}} {{CMG}} ; {{AE}} ==Overview== ==Risk Factors== * Because Friedreich’s Ataxia is a genetic diseases transmitted by autosomal recessive pat...") |
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__NOTOC__ | __NOTOC__ | ||
{{Friedreich's ataxia}} | {{Friedreich's ataxia}} | ||
{{CMG}} ; {{AE}} | {{CMG}} ; {{AE}} [[User:M Jahan|Mohamadmostafa Jahansouz M.D.]][[Mailto:mjahanso@bidmc.harvard.edu|[2]]] | ||
==Overview== | ==Overview== |
Revision as of 18:19, 15 April 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Mohamadmostafa Jahansouz M.D.[[2]]
Overview
Risk Factors
- Because Friedreich’s Ataxia is a genetic diseases transmitted by autosomal recessive pattern, the most potent risk factor in the development of Friedreich’s Ataxia is strong family history. Other risk factors are unknown.
- The risk factors for developing associated clinical conditions of Friedreich's ataxia include:
- GAA1 length
- Age of diagnosis