Titlebook: Stroke Genetics; Pankaj Sharma,James F. Meschia Book 20172nd edition The Editor(s) (if applicable) and The Author(s), under exclusive lice

總

Anal-Canal

調(diào)整

Monogenic Disorder: Fabry Disease, white matter lesions, pulvinar hyperintensity on T1-weighted images and vascular dolichoectasia. Enzyme replacement therapy has revolutionized the management of fabry disease, but its role in stroke prevention remains unclear.

延期

mitral-valve

不愿

Ornament

leniency

TEN

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASILthe different types of cerebral small vessel disease [2, 3]. Up to 1993, several families with hereditary cerebral small artery disease mimicking manifestations observed in CADASIL were reported using numerous eponyms; “Chronic familial vascular encephalopathy” [4], “Famili?re zerebrale arterioskler

Nerve-Block

Monogenic Disorder: Fabry Disease,, along with non-neurological features. Later, life-threatening complications include renal failure, heart disease, and young-onset stroke. However, patients can present with stroke before a diagnosis of fabry disease has been reached. Despite its mode of inheritance, women with fabry disease may be