A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosis Academic Article

abstract

  • © 2015 British Association of Dermatologists.Summary Autosomal recessive congenital ichthyosis (ARCI) is a group of rare, clinically heterogeneous skin disorders that affect cornification. ARCI includes lamellar ichthyosis, congenital ichthyosiform erythroderma and harlequin ichthyosis. TGM1 mutations cause > 50% of ARCI cases in the USA. We report two siblings with ARCI. They were found to carry a novel aetiological TGM1 mutation, which leads to the synthesis of multiple abnormal transcripts. These molecules resulted from three independent mechanisms: intron retention, exon skipping and activation of expand cryptic splice sites. Taken together, our findings expand the known TGM1 mutation repertoire, and provide an insight into the molecular mechanisms leading to ARCI phenotypes. These results could be useful for genetic counselling and future potential genotype-phenotype correlations.

publication date

  • 2015/10/1

keywords

  • Congenital Ichthyosiform Erythroderma
  • Exons
  • Genetic Association Studies
  • Genetic Counseling
  • Ichthyosis
  • Introns
  • Lamellar Ichthyosis
  • Mutation
  • Phenotype
  • RNA Splice Sites
  • Skin

International Standard Serial Number (ISSN)

  • 0307-6938

number of pages

  • 4

start page

  • 757

end page

  • 760