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CARASIL syndrome

MONDO:0010829

CARASIL is a hereditary cerebral small vessel disease characterized by early-onset gait disturbances, premature scalp alopecia, ischemic stroke, acute mid to lower back pain and progressive cognitive disturbances leading to severe dementia.

Also known as: CARASIL, Maeda syndrome, cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy, cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy, cerebrovascular disease with thin skin, alopecia, and disc disease, cerebrovascular disease with thin skin, alopecia, and disk disease, subcortical vascular encephalopathy, progressive

0 clinical trials for this condition and its sub-types, 0 tagged with CARASIL syndrome itself.

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