Berginer V M, Salen G, Shefer S
Department of Neurology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Neurol Clin. 1989 Feb;7(1):55-74.
Cerebrotendinous xanthomatosis is a rare familial lipid storage that is caused by a defect in bile acid synthesis. As a result, large amounts of cholestanol, the 5 alpha-dihydro derivative of cholesterol, accumulate in virtually every tissue, with extra large deposits in the nervous system, xanthomas, and bile. Clinically, progressive neurologic dysfunction, tendon xanthomas, cataracts, and atherosclerosis are commonly found. Because chenodeoxycholic acid, a primary bile acid, is almost devoid from the bile, replacement therapy (750 mg per day) suppresses abnormal bile acid synthesis, reduces elevated cholestanol synthesis and plasma concentrations, and improves neurologic function in this disease.
脑腱黄瘤病是一种罕见的家族性脂质贮积病,由胆汁酸合成缺陷引起。因此,大量的胆甾烷醇(胆固醇的5α-二氢衍生物)几乎在每个组织中蓄积,在神经系统、黄瘤和胆汁中蓄积量格外大。临床上,常见进行性神经功能障碍、肌腱黄瘤、白内障和动脉粥样硬化。由于初级胆汁酸鹅去氧胆酸几乎不存在于胆汁中,替代疗法(每天750毫克)可抑制异常胆汁酸合成,降低胆甾烷醇合成及血浆浓度升高,并改善该病的神经功能。