There are several forms of MD. Some is "X" linked and others like Frederich's Ataxia is autosomal recessive due to a flaw in chromosome 9.
With FA, two carriers of the defective gene are needed for a child to have the disorder. There is a 25% chance of a child developing it, 25% chance of being a carrier and a 50% chance of not inheriting the bad gene.
As to Thomas' condition, I think it is Hollywood Mixed Type. From what I've read, absence seizures are NOT part of the symptoms of any forms of MD or FA.
Although the weakness and poor coordination Thomas presents IS a symptom of FA in its early phases.
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