Preparing your results

Our searching services are busy right now. Your search will reload in five seconds.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Identification of MeCP2 mutations in a series of females with autistic disorder.

Pediatric neurology | Mar 28, 2003

http://www.ncbi.nlm.nih.gov/pubmed/12770674

Rett disorder and autistic disorder are both pervasive developmental disorders. Recent studies indicate that at least 80% of Rett Disorder cases are caused by mutations in the methyl-CpG-binding protein 2 (MeCP2) gene. Since there is some phenotypic overlap between autistic disorder and Rett disorder, we analyzed 69 females clinically diagnosed with autistic disorder for the presence of mutations in the MeCP2 gene. Two autistic disorder females were found to have de novo mutations in the MeCP2 gene. These data provide additional evidence of variable expression in the Rett disorder phenotype and suggest MeCP2 testing may be warranted for females presenting with autistic disorder.

Pubmed ID: 12770674 RIS Download

Mesh terms: Adolescent | Adult | Amino Acid Sequence | Autistic Disorder | Child | Child, Preschool | Chromosomal Proteins, Non-Histone | DNA-Binding Proteins | Female | Humans | Methyl-CpG-Binding Protein 2 | Molecular Sequence Data | Mutation | Repressor Proteins

Research resources used in this publication

None found

Research tools detected in this publication

None found

Data used in this publication

None found

Associated grants

  • Agency: NINDS NIH HHS, Id: NS26630
  • Agency: NINDS NIH HHS, Id: NS36768
  • Agency: NICHD NIH HHS, Id: R01 HD36701

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.