A member asked:

I want to know what's the karyotype of rett syndrome?

A doctor has provided 1 answer

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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