| Literature DB >> 9178327 |
D F Schorderet1, M Huber, R N Laurini, G Von Moos, B Gianadda, G Délèze, D Hohl.
Abstract
Autosomal recessive lamellar ichthyosis (LI) is a rare inherited disease of cornification of the skin. Recently, the gene responsible for type I LI has been identified and mutations have been described. The identification of mutations in families at risk for LI allows a precise and rapid prenatal diagnosis. A family with a previously unreported mutation is described and a prenatal diagnosis based on a simple polymerase chain reaction (PCR) approach is outlined. The molecular diagnosis was confirmed on post-mortem examination of the skin.Entities:
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Year: 1997 PMID: 9178327 DOI: 10.1002/(sici)1097-0223(199705)17:5<483::aid-pd80>3.0.co;2-4
Source DB: PubMed Journal: Prenat Diagn ISSN: 0197-3851 Impact factor: 3.050