Left hemicranial hypoplasia in 2 patients with primary progressive aphasia

Arch Neurol. 2004 Feb;61(2):265-8. doi: 10.1001/archneur.61.2.265.

Abstract

Background: Primary progressive aphasia (PPA) leads to a gradual and relatively isolated dissolution of language function. The factors that determine the selectivity of the disease process remain unknown. We had speculated that PPA may occasionally arise as a tardive manifestation of genetic or acquired vulnerabilities involving the language network of the brain.

Objective: To explore predisposing factors for PPA.

Results: In 2 patients, PPA developed with a background of mild left hemicranial hypoplasia.

Conclusion: In keeping with other observations of PPA in patients with dyslexia and childhood injury to the left temporal lobe, these 2 patients support the contention that some cases of PPA may arise in settings where the language network has become a locus of least resistance.

Publication types

  • Clinical Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Activities of Daily Living
  • Adult
  • Aphasia, Primary Progressive / pathology*
  • Aphasia, Primary Progressive / psychology
  • Apolipoproteins E / genetics
  • Brain / pathology*
  • Cognition Disorders / etiology
  • Cognition Disorders / pathology
  • Cranial Fossa, Middle / pathology
  • Electroencephalography
  • Epilepsy / complications
  • Female
  • Functional Laterality / physiology
  • Humans
  • Language
  • Male
  • Middle Aged
  • Nerve Degeneration / etiology
  • Nerve Degeneration / pathology
  • Tomography, Emission-Computed, Single-Photon
  • Tomography, X-Ray Computed

Substances

  • Apolipoproteins E