Work

Autosomal recessive epidermolysis bullosa simplex due to compound heterozygous mutations in the DST gene: the first Italian case and literature review

Year: 2025

Type: article

Abstract: Epidermolysis bullosa simplex (EBS), the most common type of EB, is characterized by skin fragility and blister formation within the basal epidermal layer. Most cases are due to autosomal dominant mutations in the keratin genes, KRT5 and KRT14. However, mutations in different genes are responsible for other EBS subtypes. We describe the clinical and molecular features of the first Italian child with autosomal recessive localized EBS due to mutations in the DST gene, encoding the BP230/BPAG1-e protein of hemidesmosomes. Molecular genetic analysis identified compound heterozygous DST nonsense variants, allowing the exclusion of a sporadic case of dominant EBS due to a de novo KRT5/KRT14 mutation. A literature review retrieved members from 20 families from Middle Eastern and South Asian countries presenting with DST-mutated EBS. In addition to illustrating the clinical features of this EBS variant, our case shows the relevance of genetic diagnosis to distinguish EBS subtypes due to different inheritance modes, thereby providing families with appropriate genetic counseling.

Source: Dermatology Reports

DOI: 10.4081/dr.2025.10206

Authors: Andrea Diociaiuti, Ruggiero Davide Zingarelli, Dario Francesco D'Urso, Giovanna Zambruno, May El Hachem

Institutions: Bambino Gesù Children's Hospital, Università Cattolica del Sacro Cuore

Language: English

Topic: Skin and Cellular Biology Research

Subfield: Cell Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: gold

Estimated APC paid: $539