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Petar Brlek, MD, PhD Candidate, Medical Genetics Resident

Cerebrotendinous xanthomatosis (CTX) is a genetic disorder of the cholesterol metabolic pathway, most often associated with variants in the CYP27A1 gene. The dysregulation of cholesterol metabolism results in the accumulation of metabolites such as cholestanol, which has a predilection for neuronal tissue and tendons. The condition is treatable with chenodeoxycholic acid (CDCA), which halts the production of these metabolites. Early diagnosis and treatment initiation in CTX patients is of great importance, as a significant reversal of disease progression can be achieved.