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Review Question - QID 101694

Friedreich Ataxia Introduction Autosomal recessive QID: 101694 (M1.NE.15.30)
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QID 101694 (Type "101694" in App Search)
An 8-year-old boy is referred to your neurology clinic with the chief complaint of "trouble walking." His mother believes her son's condition has gradually worsened over the past several months with the recent development of difficulty coordinating his arms. Physical examination is notable for an ataxic gait, nystagmus, ...
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