Hereditary sensory neuropathy with deafness and dementia: a clinical and neuroimaging study

Eur J Neurol. 1999 May;6(3):357-61. doi: 10.1046/j.1468-1331.1999.630357.x.

Abstract

We describe three sibling patients with autosomal dominantly inherited sensory neuropathy, sensorineural hearing loss and dementia. The features of cognitive-behavioral deficits in the patients, including executive dysfunction, apathy, indifference and inattention, were consistent with a frontal lobe dysfunction. Magnetic resonance imaging showed a diffuse brain atrophy. A fluorodeoxyglucose positron emission tomography in one patient and a single photon emission computed tomography in another demonstrated a glucose hypometabolism or a hypoperfusion in the medial frontal and thalamic regions. Primary frontal involvement or frontal dysfunction secondary to thalamic lesions may contribute to the nature of dementia in these patients.

Publication types

  • Case Reports

MeSH terms

  • Deafness / complications*
  • Deafness / genetics
  • Deafness / pathology*
  • Dementia / complications*
  • Dementia / genetics
  • Dementia / pathology*
  • Female
  • Frontal Lobe / diagnostic imaging
  • Frontal Lobe / pathology
  • Hereditary Sensory and Autonomic Neuropathies / complications*
  • Hereditary Sensory and Autonomic Neuropathies / genetics
  • Hereditary Sensory and Autonomic Neuropathies / pathology*
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Pedigree
  • Thalamus / diagnostic imaging
  • Thalamus / pathology
  • Tomography, Emission-Computed