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KEY FACTS
Terminology
Imaging
Top Differential Diagnoses
Pathology
Clinical Issues
TERMINOLOGY
Abbreviations
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
Definitions
Hereditary small-vessel disease due to mutations in NOTCH3 gene on chromosome 19, which causes stroke in young to middle-aged adults
IMAGING
General Features
CT Findings
MR Findings
Ultrasonographic Findings
Angiographic Findings
Nuclear Medicine Findings
Imaging Recommendations
DIFFERENTIAL DIAGNOSIS
PATHOLOGY
General Features
Gross Pathologic & Surgical Features
Microscopic Features
CLINICAL ISSUES
Presentation
Demographics
Natural History & Prognosis
Treatment
DIAGNOSTIC CHECKLIST
Consider
Image Interpretation Pearls
Selected References
Goldstein ED et al: Intracranial high-resolution vessel wall imaging in CADASIL. Neurology. 94(23):1040-41, 2020
Sun C et al: Deep gray matter iron deposition and its relationship to clinical features in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy patients: A 7.0-T magnetic resonance imaging study. Stroke. 51(6):1750-7, 2020
Tábuas-Pereira M et al: Headache intensity is associated with increased white matter lesion burden in CADASIL patients. J Clin Neurosci. 73:179-82, 2020
Ayrignac X et al: Adult-onset genetic leukoencephalopathies: A MRI pattern-based approach in a comprehensive study of 154 patients. Brain. 138(Pt 2):284-92, 2015
Bianchi S et al: CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients. J Neurol. 262(1):134-41, 2015
De Guio F et al: White matter edema at the early stage of cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Stroke. 46(1):258-61, 2015
De Guio F et al: Decreased T1 contrast between gray matter and normal-appearing white matter in CADASIL. AJNR Am J Neuroradiol. 35(1):72-6, 2014
De Guio F et al: Loss of venous integrity in cerebral small vessel disease: a 7-T MRI study in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Stroke. 45(7):2124-6, 2014
Chabriat H et al: Cadasil. Lancet Neurol. 8(7):643-53, 2009
Reyes S et al: Apathy: a major symptom in CADASIL. Neurology. 72(10):905-10, 2009
Liem MK et al: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: progression of MR abnormalities in prospective 7-year follow-up study. Radiology. 249(3):964-71, 2008
Piccirillo G et al: Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Eur J Neurol. 15(11):1216-21, 2008
Scheid R et al: Cysteine-sparing notch3 mutations: cadasil or cadasil variants? Neurology. 71(10):774-6, 2008
Rufa A et al: Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Stroke. 38(2):276-80, 2007
Buffon F et al: Cognitive profile in CADASIL. J Neurol Neurosurg Psychiatry. 77(2):175-80, 2006
Opherk C et al: Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers. Stroke. 37(11):2684-9, 2006
Singhal S et al: The spatial distribution of MR imaging abnormalities in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and their relationship to age and clinical features. AJNR Am J Neuroradiol. 26(10):2481-7, 2005
Opherk C et al: Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients. Brain. 127(Pt 11):2533-9, 2004
Peters N et al: A two-year clinical follow-up study in 80 CADASIL subjects: progression patterns and implications for clinical trials. Stroke. 35(7):1603-8, 2004
Tuominen S et al: Positron emission tomography examination of cerebral blood flow and glucose metabolism in young CADASIL patients. Stroke. 35(5):1063-7, 2004
Dong Y et al: Yield of screening for CADASIL mutations in lacunar stroke and leukoaraiosis. Stroke. 34(1):203-5, 2003
Lesnik Oberstein SA et al: Incipient CADASIL. Arch Neurol. 60(5):707-12, 2003
Lesnik Oberstein SA et al: Myocardial infarction in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Medicine (Baltimore). 82(4):251-6, 2003
Schon F et al: "CADASIL coma": an underdiagnosed acute encephalopathy. J Neurol Neurosurg Psychiatry. 74(2):249-52, 2003
Tatsch K et al: Cortical hypometabolism and crossed cerebellar diaschisis suggest subcortically induced disconnection in CADASIL: an 18F-FDG PET study. J Nucl Med. 44(6):862-9, 2003
van den Boom R et al: Cerebral hemodynamics and white matter hyperintensities in CADASIL. J Cereb Blood Flow Metab. 23(5):599-604, 2003
Auer DP et al: Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison. Radiology. 218(2):443-51, 2001
Bruening R et al: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: decrease in regional cerebral blood volume in hyperintense subcortical lesions inversely correlates with disability and cognitive performance. AJNR Am J Neuroradiol. 22(7):1268-74, 2001
Chabriat H et al: Cerebral hemodynamics in CADASIL before and after acetazolamide challenge assessed with MRI bolus tracking. Stroke. 31(8):1904-12, 2000
Desmond DW et al: The natural history of CADASIL: a pooled analysis of previously published cases. Stroke. 30(6):1230-3, 1999
Davous P: CADASIL: a review with proposed diagnostic criteria. Eur J Neurol. 5(3):219-233, 1998
Dichgans M et al: The phenotypic spectrum of CADASIL: clinical findings in 102 cases. Ann Neurol. 44(5):731-9, 1998
Tournier-Lasserve E et al: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat Genet. 3(3):256-9, 1993
Related Anatomy
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Related Differential Diagnoses
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References
Tables
Tables
KEY FACTS
Terminology
Imaging
Top Differential Diagnoses
Pathology
Clinical Issues
TERMINOLOGY
Abbreviations
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
Definitions
Hereditary small-vessel disease due to mutations in NOTCH3 gene on chromosome 19, which causes stroke in young to middle-aged adults
IMAGING
General Features
CT Findings
MR Findings
Ultrasonographic Findings
Angiographic Findings
Nuclear Medicine Findings
Imaging Recommendations
DIFFERENTIAL DIAGNOSIS
PATHOLOGY
General Features
Gross Pathologic & Surgical Features
Microscopic Features
CLINICAL ISSUES
Presentation
Demographics
Natural History & Prognosis
Treatment
DIAGNOSTIC CHECKLIST
Consider
Image Interpretation Pearls
Selected References
Goldstein ED et al: Intracranial high-resolution vessel wall imaging in CADASIL. Neurology. 94(23):1040-41, 2020
Sun C et al: Deep gray matter iron deposition and its relationship to clinical features in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy patients: A 7.0-T magnetic resonance imaging study. Stroke. 51(6):1750-7, 2020
Tábuas-Pereira M et al: Headache intensity is associated with increased white matter lesion burden in CADASIL patients. J Clin Neurosci. 73:179-82, 2020
Ayrignac X et al: Adult-onset genetic leukoencephalopathies: A MRI pattern-based approach in a comprehensive study of 154 patients. Brain. 138(Pt 2):284-92, 2015
Bianchi S et al: CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients. J Neurol. 262(1):134-41, 2015
De Guio F et al: White matter edema at the early stage of cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Stroke. 46(1):258-61, 2015
De Guio F et al: Decreased T1 contrast between gray matter and normal-appearing white matter in CADASIL. AJNR Am J Neuroradiol. 35(1):72-6, 2014
De Guio F et al: Loss of venous integrity in cerebral small vessel disease: a 7-T MRI study in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Stroke. 45(7):2124-6, 2014
Chabriat H et al: Cadasil. Lancet Neurol. 8(7):643-53, 2009
Reyes S et al: Apathy: a major symptom in CADASIL. Neurology. 72(10):905-10, 2009
Liem MK et al: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: progression of MR abnormalities in prospective 7-year follow-up study. Radiology. 249(3):964-71, 2008
Piccirillo G et al: Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Eur J Neurol. 15(11):1216-21, 2008
Scheid R et al: Cysteine-sparing notch3 mutations: cadasil or cadasil variants? Neurology. 71(10):774-6, 2008
Rufa A et al: Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Stroke. 38(2):276-80, 2007
Buffon F et al: Cognitive profile in CADASIL. J Neurol Neurosurg Psychiatry. 77(2):175-80, 2006
Opherk C et al: Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers. Stroke. 37(11):2684-9, 2006
Singhal S et al: The spatial distribution of MR imaging abnormalities in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and their relationship to age and clinical features. AJNR Am J Neuroradiol. 26(10):2481-7, 2005
Opherk C et al: Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients. Brain. 127(Pt 11):2533-9, 2004
Peters N et al: A two-year clinical follow-up study in 80 CADASIL subjects: progression patterns and implications for clinical trials. Stroke. 35(7):1603-8, 2004
Tuominen S et al: Positron emission tomography examination of cerebral blood flow and glucose metabolism in young CADASIL patients. Stroke. 35(5):1063-7, 2004
Dong Y et al: Yield of screening for CADASIL mutations in lacunar stroke and leukoaraiosis. Stroke. 34(1):203-5, 2003
Lesnik Oberstein SA et al: Incipient CADASIL. Arch Neurol. 60(5):707-12, 2003
Lesnik Oberstein SA et al: Myocardial infarction in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Medicine (Baltimore). 82(4):251-6, 2003
Schon F et al: "CADASIL coma": an underdiagnosed acute encephalopathy. J Neurol Neurosurg Psychiatry. 74(2):249-52, 2003
Tatsch K et al: Cortical hypometabolism and crossed cerebellar diaschisis suggest subcortically induced disconnection in CADASIL: an 18F-FDG PET study. J Nucl Med. 44(6):862-9, 2003
van den Boom R et al: Cerebral hemodynamics and white matter hyperintensities in CADASIL. J Cereb Blood Flow Metab. 23(5):599-604, 2003
Auer DP et al: Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison. Radiology. 218(2):443-51, 2001
Bruening R et al: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: decrease in regional cerebral blood volume in hyperintense subcortical lesions inversely correlates with disability and cognitive performance. AJNR Am J Neuroradiol. 22(7):1268-74, 2001
Chabriat H et al: Cerebral hemodynamics in CADASIL before and after acetazolamide challenge assessed with MRI bolus tracking. Stroke. 31(8):1904-12, 2000
Desmond DW et al: The natural history of CADASIL: a pooled analysis of previously published cases. Stroke. 30(6):1230-3, 1999
Davous P: CADASIL: a review with proposed diagnostic criteria. Eur J Neurol. 5(3):219-233, 1998
Dichgans M et al: The phenotypic spectrum of CADASIL: clinical findings in 102 cases. Ann Neurol. 44(5):731-9, 1998
Tournier-Lasserve E et al: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat Genet. 3(3):256-9, 1993
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