Classic cerebrotendinous xanthomatosis (CTX; OMIM #213700) manifests with chronic diarrhea, juvenile cataracts, tendon xanthomas and neurological symptoms. It is due to biallelic inactivation of CYP27A1 wich leads to cholestanol accumulation in the central nervous system, eyes and tendons. Less commonly, the disease can present in young adults as spastic paraparesis in the absence of xanthomas. We report a 38-year old woman who presented with chronic diarrhea and progressive spastic paraparesis in her twenties. Brain magnetic resonance imaging (MRI) showed cerebral atrophy with diffuse periventricular white matter hyperintensities. Spinal MRI was normal. CYP27A1 gene sequencing confirmed the diagnosis of CTX. Chenodeoxycholic acid (CDCA) tr...
Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive disease due to defective activity...
BACKGROUND: Cerebrotendinous xanthomatosis (CTX) is an autosomal recessively inherited inborn error ...
International audienceCerebrotendinous xanthomatosis (CTX) is among the few inherited neurometabolic...
Cerebrotendinous Xanthomatosis (CTX) is an autosomal recessive defect of the alternative pathway of ...
Cerebrotendinous Xanthomatosis(CTX) is an uncommon autosomal recessive disorder in which there is ac...
Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive lipid storage disorder due to a d...
Cerebrotendinous xanthomatosis (CTX) is a rare neurometabolic disease due to defective activity of s...
We describe a patient with cerebrotendinous xanthomatosis (CTX) who saw a Rheumatologist because of ...
Cerebrotendinous xanthomatosis (CTX) is an autosomal-recessive disorder of lipid storage caused by m...
Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive inborn error of bile acids synthesis ...
Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive lipid storage disease caused by a def...
peer reviewedCerebrotendinous xanthomatosis (CTX) is a rare and treatable autosomal recessive diseas...
Cerebrotendinous xanthomatosis (CTX) is a rare hereditary neuro-metabolic disease in which depositio...
Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive lipid storage disease caused by a def...
Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive disease due to defective activity...
BACKGROUND: Cerebrotendinous xanthomatosis (CTX) is an autosomal recessively inherited inborn error ...
International audienceCerebrotendinous xanthomatosis (CTX) is among the few inherited neurometabolic...
Cerebrotendinous Xanthomatosis (CTX) is an autosomal recessive defect of the alternative pathway of ...
Cerebrotendinous Xanthomatosis(CTX) is an uncommon autosomal recessive disorder in which there is ac...
Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive lipid storage disorder due to a d...
Cerebrotendinous xanthomatosis (CTX) is a rare neurometabolic disease due to defective activity of s...
We describe a patient with cerebrotendinous xanthomatosis (CTX) who saw a Rheumatologist because of ...
Cerebrotendinous xanthomatosis (CTX) is an autosomal-recessive disorder of lipid storage caused by m...
Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive inborn error of bile acids synthesis ...
Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive lipid storage disease caused by a def...
peer reviewedCerebrotendinous xanthomatosis (CTX) is a rare and treatable autosomal recessive diseas...
Cerebrotendinous xanthomatosis (CTX) is a rare hereditary neuro-metabolic disease in which depositio...
Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive lipid storage disease caused by a def...
Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive disease due to defective activity...
BACKGROUND: Cerebrotendinous xanthomatosis (CTX) is an autosomal recessively inherited inborn error ...
International audienceCerebrotendinous xanthomatosis (CTX) is among the few inherited neurometabolic...