Recessive dystrophic epidermolysis bullosa caused by a novel COL7A1 variant with isodisomy

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作者
Yo Niida
Azusa Kobayashi
Sumihito Togi
Hiroki Ura
机构
[1] Kanazawa Medical University Hospital,Center for Clinical Genomics
[2] Kanazawa Medical University,Division of Genomic Medicine, Department of Advanced Medicine, Medical Research Institute
[3] Kanazawa Medical University,Department of Pediatrics
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Human Genome Variation | / 10卷
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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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