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Fig. 1 | BMC Dermatology

Fig. 1

From: A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report

Fig. 1

Clinical features in the 28-year-old female with epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia. This patient is originated from the Azorean island of São Miguel (Portugal). a Diffuse alopecia of the scalp, (b) Sparse and hemorrhagic blistering of the hand and onychodystrophy, and (c) Oral cavity abnormalities, such as caries and enamel hypoplasia

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