Genetics: Rett syndrome is a severe neurodevelopmental disorder that arises from mutations in the x-linked mecp2 gene. It is almost exclusively seen in girls due to the predominant occurrence of the mutations on the paternal x-chromosome. For more info, consult with a geneticist.
Answered 1/3/2014
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A doctor has provided 1 answer
A doctor has provided 1 answer
A doctor has provided 1 answer
A doctor has provided 1 answer
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