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CADASIL

More information in Books or onNLM PubMed
Definition: A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146)      Other names Dementia, Hereditary Multi Infarct Type; Dementia, Hereditary Multi-Infarct Type; Cerebral Autosomal Dominant Arteriopathy with Subc; Cerebral Arteriopathy with Subcortical Infarcts an; CADASILM
 
SubstanceCAS Registry & nameCategoriesSource
Familial vascular leukoencephalopathy  0   *CADASIL.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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