Friedreich's ataxia risk factors: Difference between revisions
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==Risk Factors== | ==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. | * 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: | * The risk factors for developing associated clinical conditions of Friedreich's ataxia include:<ref name="pmid2579318">{{cite journal |vauthors=Lazo JS, Hait WN, Kennedy KA, Braun ID, Meandzija B |title=Enhanced bleomycin-induced DNA damage and cytotoxicity with calmodulin antagonists |journal=Mol. Pharmacol. |volume=27 |issue=3 |pages=387–93 |date=March 1985 |pmid=2579318 |doi= |url=}}</ref> | ||
** GAA1 length | ** GAA1 length | ||
** Age of diagnosis | ** Age of diagnosis | ||
Revision as of 17:07, 19 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:[1]
- GAA1 length
- Age of diagnosis