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Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes
Author(s) -
Gail E. Herman
Publication year - 2003
Publication title -
human molecular genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.811
H-Index - 276
eISSN - 1460-2083
pISSN - 0964-6906
DOI - 10.1093/hmg/ddg072
Subject(s) - biology , cholesterol , chondrodysplasia punctata , biosynthesis , farnesyl diphosphate farnesyltransferase , smith–lemli–opitz syndrome , metabolic disorder , genetics , endocrinology , medicine , enzyme , gene , biochemistry , farnesyltransferase , prenylation , 7 dehydrocholesterol reductase , reductase
Since 1998, five disorders involving enzyme defects in post-squalene cholesterol biosynthesis have been identified-desmosterolosis, X-linked dominant chondrodysplasia punctata, CHILD syndrome, lathosterolosis, and hydrops-ectopic calcification-moth-eaten skeletal dysplasia. They join the most common cholesterol biosynthetic disorder, Smith-Lemli-Opitz syndrome, whose underlying defect was identified in 1993. All are associated with major developmental malformations that are unusual for metabolic disorders. The existence of mouse models for five of these disorders is beginning to enable more detailed developmental and in vitro studies examining the mechanisms involved in disease pathogenesis. In this review, an overview of the cholesterol biosynthetic pathway will be presented. Clinical features of the human disorders and mouse models of post-squalene cholesterol biosynthesis will then be discussed.

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