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The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.
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Rett Syndrome
Rett Syndrome
Prevalence:
~50K
neurological
Official
·
OMIM:312750
Official
·
ORPHA778
Neurodevelopmental disorder caused by mutations in MECP2. Predominantly affects girls.
Associated Genes
MECP2
Methyl-CpG Binding Protein 2
Chromosome X
X-Linked Dominant