Algorithmic approach for methyl-CpG binding protein 2 (MECP2) gene testing in patients with neurodevelopmental disabilities

J Child Neurol. 2012 Mar;27(3):346-54. doi: 10.1177/0883073811424796. Epub 2011 Nov 28.

Abstract

Methyl-CpG binding protein 2 gene (MECP2) testing is indicated for patients with numerous clinical presentations, including Rett syndrome (classic and atypical), unexplained neonatal encephalopathy, Angelman syndrome, nonspecific mental retardation, autism (females), and an X-linked family history of developmental delay. Because of this complexity, a gender-specific approach for comprehensive MECP2 gene testing is described. Briefly, sequencing of exons 1 to 4 of MECP2 is recommended for patients with a Rett syndrome phenotype, unexplained neonatal encephalopathy, an Angelman syndrome phenotype (with negative 15q11-13 analysis), nonspecific mental retardation, or autism (females). Additional testing for large-scale MECP2 deletions is recommended for patients with Rett syndrome or Angelman syndrome phenotypes (with negative 15q11-13 analysis) following negative sequencing. Alternatively, testing for large-scale MECP2 duplications is recommended for males presenting with mental retardation, an X-linked family history of developmental delay, and a significant proportion of previously described clinical features (particularly a history of recurrent respiratory infections).

Publication types

  • Review

MeSH terms

  • Algorithms*
  • Brain Diseases / complications
  • Brain Diseases / genetics*
  • Chromosomes, Human, Pair 15 / genetics
  • DNA Mutational Analysis
  • Developmental Disabilities / complications
  • Developmental Disabilities / genetics*
  • Exons / genetics
  • Female
  • Humans
  • Male
  • Methyl-CpG-Binding Protein 2 / genetics*
  • Mutation / genetics*
  • Sex Factors

Substances

  • MECP2 protein, human
  • Methyl-CpG-Binding Protein 2