Kindler syndrome: extension of FERMT1 mutational spectrum and natural history Articles uri icon

publication date

  • November 2011

start page

  • 1204

end page

  • 1212

issue

  • 11

volume

  • 32

international standard serial number (ISSN)

  • 1059-7794

electronic international standard serial number (EISSN)

  • 1098-1004

abstract

  • Mutations in the FERMT1 gene (also known as KIND1), encoding the focal adhesion protein kindlin-1, underlie the Kindler syndrome (KS), an autosomal recessive skin disorder with an intriguing progressive phenotype comprising skin blistering, photosensitivity, progressive poikiloderma with extensive skin atrophy, and propensity to skin cancer. Herein we review the clinical and genetic data of 62 patients, and delineate the natural history of the disorder, for example, age at onset of symptoms, or risk of malignancy. Although most mutations are predicted to lead to premature termination of translation, and to loss of kindlin-1 function, significant clinical variability is observed among patients. There is an association of FERMT1 missense and in-frame deletion mutations with milder disease phenotypes, and later onset of complications. Nevertheless, the clinical variability is not fully explained by genotype-phenotype correlations. Environmental factors and yet unidentified modifiers may play a role. Better understanding of the molecular pathogenesis of KS should enable the development of prevention strategies for disease complications.

keywords

  • fermt1; epidermolysis bullosa; kindlin; poikiloderma; blister; fermitin; gene mutation