Clinical Feature and Genetics in Rett Syndrome: A Report on Iranian Patients Publisher



Karimzadeh P^{1, 2} ; Kheirollahi M³ ; Houshmand SM⁴ ; Dadgar S⁵ ; Aryani O⁴ ; Yaghini O⁶ Show Affiliations
Source: Iranian Journal of Child Neurology Published:2019

Abstract

Rett syndrome is characterized by normal development for the first 6-18 months of life followed by the loss of fine and gross motor skills and the ability to engage in social interaction. In most patients, mutations are found in methyl CpG-binding protein 2 (MECP2) gene. We investigated the relation between Rett clinical diagnosis and mutations in MECP2. Materials & Methods Children suspected of Rett syndrome were invited to participate in this study. Twenty-three patients from the Mofid Hospital, Tehran, Iran suffered from classic Rett syndrome diagnostic criteria were enrolled in 2012. The severity of symptoms was assessed for all of them. The peripheral blood samples were collected in EDTA tubes and the genomic DNA was extracted using standard salting out method. The mutation of MEPC2 gene was studied using DNA sequencing method. Results Overall, 11(47.8%) patients had MECP2 gene mutation, while 12 cases (52.2%) had no mutations. Changes in genetics were associated with phenotypical manifestations. The most prevalent mutation was p.v288 mainly associated with partially or uncontrolled seizures. Conclusion For the first time, we studies the Rett syndrome in terms of clinical manifestations and genetic changes in Iran. © 2019, Iranian Child Neurology Society. All rights reserved.