[Microangiopathy CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)

Przeglad Lekarski
|April 26, 2018
PubMed

Insights

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a generalized small vessel disease. Early diagnosis through genetic testing and biopsy is crucial to avoid misdiagnosis of white matter changes.

Area of Science:

  • Neurology
  • Genetics
  • Vascular Biology

Background:

  • Small cerebral vessel diseases are increasingly diagnosed via neuroimaging.
  • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a prominent example, presenting with stroke, dementia, and migraines.
  • Symptoms often appear in mid-adulthood, independent of typical vascular risk factors.

Purpose of the Study:

  • To highlight the diagnostic challenges and importance of recognizing CADASIL.
  • To differentiate CADASIL from other white matter lesions detected by neuroimaging.

Main Methods:

  • Genetic testing for NOTCH3 gene mutations.
  • Microscopic examination of blood vessels from skin or skin-muscle biopsy.
  • Analysis of neuroimaging findings, including white matter hyperintensities and ischemic foci.

Main Results:

  • CADASIL is caused by NOTCH3 gene mutations, leading to small artery degeneration.
  • Neuroimaging reveals disseminated white matter changes, sometimes asymptomatic or misdiagnosed.
  • Diagnosis relies on genetic and histopathological evidence.

Conclusions:

  • Increased neuroimaging detection of white matter changes necessitates awareness of CADASIL.
  • Knowledge of CADASIL and other microangiopathies is essential for accurate diagnosis.
  • Avoiding diagnostic errors in small vessel diseases is critical for patient management.

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