Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): A rare cause of ischemic stroke in young

Authors

  • Gautam B Kale Anandrishiji Hospital and Medical Research Centre, Ahmednagar
  • Prajnya Ranganath Nizam’s Institute of Medical Sciences (NIMS), Hyderabad
  • Jagarlapudi M K Murthy RENOVA INSTITUTE OF NEUROLOGICAL SCIENCES

DOI:

https://doi.org/10.54029/2024muu

Keywords:

CARASIL, Lacunar stroke, Scalp alopecia, lumbosacral spondylosis, HTRA1 gene

Abstract

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is the second known genetic form of cerebral small vessel disease after cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). It is a very rare single gene disorder affecting cerebral small blood vessels. Diagnosis of CARASIL should strongly be suspected in a young non-hypertensive patient with lacunar stroke in the basal ganglia and brainstem and alopecia limited to scalp.

Published

2024-10-05

Issue

Section

Case Report