Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia

Neurology. 2005 Nov 8;65(9):1364-9. doi: 10.1212/01.wnl.0000182813.94713.ee. Epub 2005 Oct 12.

Abstract

Background: Mutations of oligophrenin 1, one of the first genes identified in nonspecific X-linked mental retardation (MRX), have been described in patients with moderate to severe cognitive impairment and predominant cerebellar hypoplasia, in the vermis.

Objective: To further delineate the phenotypic and mutational spectrum of the syndrome, by screening oligophrenin 1 in two cohorts of male patients with mental retardation (MR) with or without known posterior fossa anomalies.

Methods: Clinical examination, cognitive testing, MRI studies, and mutational analysis (denaturing gradient gel electrophoresis and direct sequencing) on blood lymphocytes were performed in 213 unrelated affected individuals: 196 patients classified as MRX and 17 patients with MR and previously detected cerebellar anomalies.

Results: Four novel oligophrenin 1 mutations were identified. In the MRX group, two nonsense mutations were detected. In the MR group, two mutations were found: a deletion of exons 16 to 17 and a splice site mutation. All patients shared characteristic clinical, radiologic, and distinctive features with a degree of intrafamilial variability in motor and cognitive deficits.

Conclusions: Oligophrenin 1 mutations were found in 12% (2/17) of individuals with mental retardatin and known cerebellar anomalies and in 1% (2/196) of the X-linked mental retardation group.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Alternative Splicing / genetics
  • Cerebellar Diseases / diagnosis
  • Cerebellar Diseases / genetics*
  • Cerebellar Diseases / physiopathology
  • Cerebellum / abnormalities*
  • Cerebellum / metabolism
  • Cerebellum / physiopathology
  • Child
  • Child, Preschool
  • Codon, Nonsense / genetics
  • Cohort Studies
  • Cytoskeletal Proteins / genetics*
  • DNA Mutational Analysis
  • Facial Asymmetry / diagnosis
  • Facial Asymmetry / genetics
  • GTPase-Activating Proteins / genetics*
  • Gene Deletion
  • Genetic Testing
  • Genotype
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mental Retardation, X-Linked / complications*
  • Mental Retardation, X-Linked / genetics*
  • Mental Retardation, X-Linked / physiopathology
  • Mutation / genetics
  • Nervous System Malformations / diagnosis
  • Nervous System Malformations / genetics*
  • Nervous System Malformations / physiopathology
  • Nuclear Proteins / genetics*
  • Pedigree
  • Phenotype
  • RNA Splice Sites / genetics

Substances

  • Codon, Nonsense
  • Cytoskeletal Proteins
  • GTPase-Activating Proteins
  • Nuclear Proteins
  • OPHN1 protein, human
  • RNA Splice Sites

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