Preserved speech variants of the Rett syndrome: Molecular and clinical analysis

Michael Rauchman, William H. Hoffman, James D. Hanna, Anita S. Kulharya, Ramon E Figueroa Ortiz, Jing Yang, Cathy M. Tuck-Miller

Research output: Contribution to journalArticle

97 Citations (Scopus)

Abstract

Mutations in the MECP2 gene cause the severe neurodevelopmental disorder called Rett syndrome. Preliminary evidence suggests that MECP2 may be involved in a broader phenotype than classical Rett syndrome including preserved speech variants (PSV). Here we report clinical and mutation analysis of 18 PSV patients. Ten of them had a MECP2 mutation (55%). The clinical features of these girls have been characterized and two subgroups defined. All of them had slow recovery of verbal and praxic abilities, evident autistic behavior, and normal head circumference. Six were overweight, often obese, had kyphosis, coarse face, and mental age of two-to-three years, and were able to speak in sentences; four had normal weight, mental age not beyond one-to-two years, and spoke in single words and two-word phrases. The course of the disorder was in stages as in classic Rett syndrome. Handwashing was present in the first years of life but often subsequently disappeared. Significantly, all mutations found in PSV are either missense or late truncating mutations. In particular, we did not find the four early truncating hot spots: R168X, R255X, R270X, R294X. These results suggest that early truncating mutations lead to a poor prognosis (classic Rett), while late truncating and missense mutations lead either to classic Rett or PSV. We hypothesize that a missense or late truncating mutation is necessary but not sufficient to produce a PSV, based on the presence of one (or more) modifier genes whose product may interact in a epistatic manner with MeCP2 protein.

Original languageEnglish (US)
Pages (from-to)14-22
Number of pages9
JournalAmerican Journal of Medical Genetics
Volume104
Issue number1
DOIs
StatePublished - Nov 15 2001

Fingerprint

Mutation
Rett Syndrome
Methyl-CpG-Binding Protein 2
Modifier Genes
Hand Disinfection
Kyphosis
Aptitude
Missense Mutation
Preserved Speech Variant Rett Syndrome
Head
Phenotype
Weights and Measures
Genes

Keywords

  • MECP2 gene
  • Modifier gene
  • PSV

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

Rauchman, M., Hoffman, W. H., Hanna, J. D., Kulharya, A. S., Figueroa Ortiz, R. E., Yang, J., & Tuck-Miller, C. M. (2001). Preserved speech variants of the Rett syndrome: Molecular and clinical analysis. American Journal of Medical Genetics, 104(1), 14-22. https://doi.org/10.1002/ajmg.10005

Preserved speech variants of the Rett syndrome : Molecular and clinical analysis. / Rauchman, Michael; Hoffman, William H.; Hanna, James D.; Kulharya, Anita S.; Figueroa Ortiz, Ramon E; Yang, Jing; Tuck-Miller, Cathy M.

In: American Journal of Medical Genetics, Vol. 104, No. 1, 15.11.2001, p. 14-22.

Research output: Contribution to journalArticle

Rauchman, M, Hoffman, WH, Hanna, JD, Kulharya, AS, Figueroa Ortiz, RE, Yang, J & Tuck-Miller, CM 2001, 'Preserved speech variants of the Rett syndrome: Molecular and clinical analysis', American Journal of Medical Genetics, vol. 104, no. 1, pp. 14-22. https://doi.org/10.1002/ajmg.10005
Rauchman, Michael ; Hoffman, William H. ; Hanna, James D. ; Kulharya, Anita S. ; Figueroa Ortiz, Ramon E ; Yang, Jing ; Tuck-Miller, Cathy M. / Preserved speech variants of the Rett syndrome : Molecular and clinical analysis. In: American Journal of Medical Genetics. 2001 ; Vol. 104, No. 1. pp. 14-22.
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