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Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998
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Article Abstract
Mutations in the sterol 27-hydroxylase gene(CYP27)cause cerebrotendinous xanthomatosis(CTX).Early diagnosis of CTX is crucial because treatment with chenodeoxycholic acid can prevent or reverse some of the neurologic disability associated with the disease.We report the identification of three types of mutations(Arg441Trp,Arg 372 Gln,and Arg441Gln)in the CYP27 gene in five patients with suspected CTX from four unrelated families by restriction endonuclease analysis.
 
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cerebrotendinous xanthomatosis
familial
gene
genetic diagnosis,prenatal
genetic neurologic disorders
genetic testing
molecular genetics
neurologic disease,diagnoses of

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