CADASIL syndrome: Long-term follow-up on MRI

Borbely, Klaudia ✉ [Borbély, Klaudia (Radiológia), author] Orvosi Képalkotó Klinika (SU / FM / C); Radiológia Tanszék (SU / FM / C / OKK); Balogh, Hanna [Balogh, Hanna (radiológia), author]; Kardos, Ilona Blanka; Fontanini, Daniele Mariastefano [Fontanini, Daniele Mariastefano (orvostudomány), author] Cardiovascular Center (SU / FM / C); Olah, Laszlo [Oláh, László (Neurológia), author] Department of Neurology (UD); Berenyi, Ervin [Berényi, Ervin László (Radiológia), author] Orvosi Képalkotó Intézet (UD); Maurovich-Horvat, Pal [Maurovich-Horvat, Pál (kardiológia), author] Orvosi Képalkotó Klinika (SU / FM / C); Radiológia Tanszék (SU / FM / C / OKK)

English Note, Short, Rapid communications (Journal Article) Scientific
Published: IMAGING 2732-0960 14 (2) pp. 109-112 2022
  • SJR Scopus - Medicine (miscellaneous): Q4
Identifiers
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a hereditary vascular disorder inherited in an autosomal dominant manner. MRI plays a crucial role in the diagnosis and follow-up of patients. Characteristic MRI lesions include symmetric and bilateral white matter periventricular hyperintensities, lacunar infarcts and cerebral microbleeds. In our case report, we demonstrate a male patient with genetically confirmed CADASIL syndrome and the progression of symptoms with corresponding imaging findings throughout the years.
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2025-04-10 23:06