Mutations in transglutaminase 1 gene in autosomal recessive congenital ichthyosis in Egyptian families

Article type: Research Article

Authors: Shawky, R.M. | Sayed, N.S. | Elhawary, N.A.

Affiliations: Pediatrics and Genetics Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt | Medical Genetics Center, Faculty of Medicine, Ain Shams University, Cairo, Egypt. Tel.: +202 5311741; Fax: +202 2585577; E-mail: nasgenet@hotmail.com

Abstract: Autosomal recessive congenital ichthyosis (ARCI) is a rare heterogeneous keratinization disorder of the skin. It is clinically divided into 2 subtypes, lamellar ichthyosis (LI) and congenital ichthyosiformis erythroderma (CIE). We investigated forty-three ARCI Egyptian individuals in 16 severe LI, and 10 CIE families. We identified 5 alleles in two Egyptian families as having intron-5/exon-6 splice acceptor mutation recognized by the MspI restriction endonuclease. This promoted to a frequency of 9.6% for this mutation (5 splice-mutation alleles/52 alleles tested). We extended our previous dataset to update the detection of R142H mutation in 4 CIE Egyptian families and one LI phenotype (frequency of 28.8%; 15/52), whereas we still had no R141H among our Egyptian population. There was no correlation between phenotype and genotype in our study. Surprisingly, the mutant alleles detected in intron-5 acceptor splice-site were associated with the other extreme of CIE phenotypes rather than the severe LI form. We clearly demonstrated that the ARCI Egyptian families in Upper Egypt was ethnically pure and had a tendency not to be a hybrid with other populations in Lower Egypt, Delta zone and Cairo city.

Journal: Disease Markers, vol. 20, no. 6, pp. 325-332, 2004