Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patients

J Med Genet. 2008 Nov;45(11):738-44. doi: 10.1136/jmg.2008.060129. Epub 2008 Aug 26.

Abstract

Background: Haploinsufficiency of the gene encoding for transcription factor 4 (TCF4) was recently identified as the underlying cause of Pitt-Hopkins syndrome (PTHS), an underdiagnosed mental-retardation syndrome characterised by a distinct facial gestalt, breathing anomalies and severe mental retardation.

Methods: TCF4 mutational analysis was performed in 117 patients with PTHS-like features.

Results: In total, 16 novel mutations were identified. All of these proven patients were severely mentally retarded and showed a distinct facial gestalt. In addition, 56% had breathing anomalies, 56% had microcephaly, 38% had seizures and 44% had MRI anomalies.

Conclusion: This study provides further evidence of the mutational and clinical spectrum of PTHS and confirms its important role in the differential diagnosis of severe mental retardation.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Apnea* / diagnosis
  • Apnea* / genetics
  • Apnea* / pathology
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • Child
  • Child, Preschool
  • DNA Mutational Analysis*
  • DNA-Binding Proteins / genetics*
  • Face / abnormalities*
  • Face / pathology
  • Female
  • Genotype
  • Humans
  • Hyperventilation* / diagnosis
  • Hyperventilation* / genetics
  • Hyperventilation* / pathology
  • Infant
  • Intellectual Disability / diagnosis
  • Intellectual Disability / genetics*
  • Intellectual Disability / pathology
  • Male
  • Microcephaly
  • Phenotype
  • Syndrome
  • Transcription Factor 4
  • Transcription Factors / genetics*
  • Young Adult

Substances

  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • DNA-Binding Proteins
  • TCF4 protein, human
  • Transcription Factor 4
  • Transcription Factors