A Rare Case of Cerebrotendinous Xanthomatosis Associated With a Mutation on COG8 Gene
Cerebrotendinous xanthomatosis ( CTX ) is a rare hereditary disease described by a mutation in the CYP27A1 gene , which encodes the sterol 27-hydroxylase enzyme involved in the synthesis of bile acid. Accumulation of cholesterol and its metabolite, cholestanol, in multiple body organs causes the sym...
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Main Authors: | Hamed Ghoshouni MD (Author), Roham Sarmadian MD (Author), Rana Irilouzadian MD (Author), Habibe Nejad Biglari MD (Author), Abolfazl Gilani MD (Author) |
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Format: | Book |
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SAGE Publishing,
2023-04-01T00:00:00Z.
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