Schorderet D F, Huber M, Laurini R N, Von Moos G, Gianadda B, Délèze G, Hohl D
Unit of Molecular Genetics, CHUV, Switzerland.
Prenat Diagn. 1997 May;17(5):483-6. doi: 10.1002/(sici)1097-0223(199705)17:5<483::aid-pd80>3.0.co;2-4.
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.