Hereditary Cerebral Small Vessel Diseases and Stroke: A Guide for Diagnosis and Management

Author:

Guey Stéphanie12,Lesnik Oberstein Saskia A.J.3,Tournier-Lasserve Elisabeth12,Chabriat Hugues12ORCID

Affiliation:

1. CERVCO, FHU NeuroVasc, Assistance Publique des Hôpitaux de Paris and Paris University, France (S.G., E.T.-L., H.C.).

2. INSERM UMR 1141, NeuroDiderot, Université de Paris, France (S.G., E.T.-L., H.C.).

3. Department of Clinical Genetics, Leiden University Medical Center, the Netherlands (S.A.J.L.O.).

Abstract

Cerebral small vessel diseases represent a frequent cause of stroke and cognitive or motor disability in adults. A small proportion of cerebral small vessel diseases is attributable to monogenic conditions. Since the characterization in the late 1990s of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, several other monogenic conditions leading to adult-onset ischemic or hemorrhagic stroke have been described. In this practical guide, we summarize the key features that should elicit the differential diagnosis of a hereditary cerebral small vessel diseases in adult stroke patients, describe the main clinical and imaging characteristics of the major hereditary cerebral small vessel diseases that can manifest as stroke, and provide general recommendations for the clinical management of affected patients and their relatives.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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