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CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

CARASIL can cause different symptoms even with the same genetic mutation.