Literature DB >> 22561697

Novel double deletions in the MECP2 gene in Tunisian Rett patient.

Nourhene Fendri-Kriaa1, Aida Rouissi, Rania Ghorbel, Emna Mkaouar-Rebai, Neila Belguith, Naziha Gouider-Khouja, Faiza Fakhfakh.   

Abstract

Rett syndrome (RTT) is a severe neurodevelopmental disorder affecting almost exclusively girls. Rett patients present an apparently normal psychomotor development during the first 6-18 months of life. Thereafter, they show a short period of developmental stagnation followed by a rapid regression in language and motor development. RTT is currently considered as monogenic X-linked dominant disorder due to mutations in the MECP2 gene, encoding the methyl-CpG binding protein 2. The aim of this study was to perform a mutational analysis of the MECP2 gene in a classical Rett patient.The results showed the presence of a novel point mutation c.C1142T (p.P381L) and two deletions at the heterozygous state: a novel deletion c.1075delTTC (p.S359) and a known one c.1157del44 (p.L386Q fs X2) in the C-terminal region of MeCP2.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22561697     DOI: 10.1016/j.gene.2012.04.028

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  1 in total

1.  Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome.

Authors:  Christopher A Chapleau; Jane Lane; Susan M Kirwin; Carolyn Schanen; Kathy M B Vinette; Danielle Stubbolo; Patrick MacLeod; Daniel G Glaze; Kathleen J Motil; Jeffrey L Neul; Steven A Skinner; Walter E Kaufmann; Alan K Percy
Journal:  Am J Med Genet A       Date:  2013-05-21       Impact factor: 2.802

  1 in total

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