Herman G E
Children's Research Institute and Department of Pediatrics, Ohio State University, 700 Children's Dr. Rm. W403, Columbus, OH 43205, USA.
Biochim Biophys Acta. 2000 Dec 15;1529(1-3):357-73. doi: 10.1016/s1388-1981(00)00160-8.
The X-linked dominant male-lethal mouse mutations tattered and bare patches are homologous to human X-linked dominant chondrodysplasia punctata and CHILD syndrome, rare human skeletal dysplasias. These disorders also affect the skin and can cause cataracts and microphthalmia in surviving, affected heterozygous females. They have recently been shown to result from mutations in genes encoding enzymes involved in sequential steps in the conversion of lanosterol to cholesterol. This review will summarize clinical features of the disorders and describe recent biochemical and molecular investigations that have resulted in the elucidation of the involved genes and their metabolic pathway. Finally, speculations about possible mechanisms of pathogenesis will be provided.
X连锁显性致死性小鼠突变“衣衫褴褛”(tattered)和“秃斑”(bare patches)与人类X连锁显性点状软骨发育不良及先天性鱼鳞病样红皮病综合征(CHILD综合征)同源,这两种是罕见的人类骨骼发育异常疾病。这些疾病也会影响皮肤,并且在存活的患病杂合子女性中可导致白内障和小眼症。最近研究表明,它们是由参与羊毛甾醇转化为胆固醇连续步骤的酶编码基因突变引起的。本综述将总结这些疾病的临床特征,并描述最近的生化和分子研究,这些研究已阐明了相关基因及其代谢途径。最后,将对可能的发病机制进行推测。