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Published on: August 20, 2019
Recessive dystrophic epidermolysis bullosa caused by a novel COL7A1 variant with isodisomy
Yo Niida1,2, Azusa Kobayashi3, Sumihito Togi4,5
1Center for Clinical Genomics, Kanazawa Medical University Hospital, Ishikawa, Uchinada, Japan. niida@kanazawa-med.ac.jp.
Abstract:
Recessive dystrophic epidermolysis bullosa is a genetic collagen disorder characterized by skin fragility that leads to generalized severe blistering, wounds, and scarring. In this report, we present a patient with a novel COL7A1 homozygous nonsense variant, c.793C>T p.(Gln265*). Although the parents were not consanguineous, both were heterozygous carriers of the variant. Single nucleotide polymorphism (SNP) array analysis revealed an isodisomy area on 3p22.1p21.1, encompassing COL7A1, suggesting that the variant originated from a common ancestor.
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