Fig. 1From: First case report of complete paternal isodisomy of chromosome 10 harbouring a novel variant in COL17A1 that causes junctional epidermolysis bullosa intermediateClinical features, histopathological analyses and ultrastructural features of the proband. A. The neonatal features of the proband. B. The skin features of the proband at 2Â years of age. C. Limb deformity and skin features of the proband at 5Â years of ageBack to article page