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Influence of MECP2 Gene Mutation and X-Chromosome Inactivation on the Rett Syndrome Phenotype

Department of Pediatrics Seoul National University College of Medicine, Seoul, Korea

Hee Hwang, MD

Department of Pediatrics Seoul National University College of Medicine, Seoul, Korea

Yong Seung Hwang, MD

Department of Pediatrics Seoul National University College of Medicine, Seoul, Korea

Hee Jung Cheong, MD

Department of Pediatrics National Health Insurance Cooperation Ilsan Hospital, Kyonggi, Korea

Ki Joong Kim, MD

Department of Pediatrics Seoul National University College of Medicine, Seoul, Korea, pednr{at}plaza.snu.ac.kr

To date, approximately 200 different mutations in the MECP2 gene have been identified. We analyzed the entire coding sequence of the MECP2 gene and the X-chromosome inactivation pattern in 42 sporadic cases of Rett syndrome. Of the 42 patients, 30 had pathogenic mutations, including 14 different mutations: 9 missense mutations, 4 nonsense mutations, and 1 frameshift mutation. One was a novel mutation (S134P). There was a tendency for patients who had a nonsense mutation in the transcriptional repression domain region to show earlier onset of regression and more severe language retardation than patients with a mutation in the methyl-CpG binding domain region. However, the parameters of clinical severity were variable among patients with the same type of mutation, depending on the pattern of X-chromosome inactivation. This study suggests that the X-chromosome inactivation pattern can modify the phenotype of Rett syndrome, which is primarily determined by the type and site of MECP2 gene mutation. ( J Child Neurol 2004;19:503—508).

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