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Virtually all cases of RTT are caused by a mutation in the methyl CpG binding protein 2 gene (MECP2).

Rett Syndrome (RTT) is a rare genetic disorder, namely, it results from an alteration in one or more genes.

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The diagnosis of classic Rett Syndrome (RTT) rests on clinical diagnosis criteria.

There is no cure for Rett Syndrome (RTT). Treatment is mainly symptomatic and supportive.

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