Objectives: Rett syndrome is an X linked dominant neurodevelopmental disorder which almost exclusively affects females. The syndrome is usually caused by mutations in gene, which is a nuclear protein that selectively binds CpG dinucleotides in the genome.
Materials & Methods: To provide further insights into the distribution of mutations in gene, we investigated 24 females with clinical characters of Rett syndrome referred to Alzahra University Hospital in Isfahan, Iran during 2015-2017. We sequenced the entire coding region and splice sites for detection of point mutations in this gene. Freely available programs including JALVIEW, SIFT, and PolyPhen were used to find out the damaging effects of unknown mutations.
Results: Direct sequencing revealed mutations in 13 of the 24 patients. We identified in 13 patients, 10 different mutations in gene. Three of these mutations have not been reported elsewhere and are most likely pathogenic.
Conclusion: Defects in gene play an important role in pathogenesis of Rett syndrome. Mutations in gene can be found in the majority of Iranian RTT patients. We failed to identify mutations in gene in 46% of our patients. For these patients, further molecular analysis might be necessary.
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