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A Case of Epidermolysis Bullosa Simplex (Dowling-Meara 1 Type) in Newborn |
Gahyun Hong, Minsun Choi |
Neonatal Med. 2022;29(4):130-134. Published online November 30, 2022 DOI: https://doi.org/10.5385/nm.2022.29.4.130 |
A Case of Epidermolysis Bullosa Simplex (Dowling-Meara 1 Type) in Newborn Epidermolysis bullosa nevus arising in a patient with Dowling–Meara type epidermolysis bullosa simplex: Case report and literature review Epidermolysis bullosa nevus arising in a patient with Dowling-Meara type epidermolysis bullosa simplex with a novel K5 mutation Epidermolysis bullosa simplex, Dowling-Meara type with eruptive nevi Epidermolysis bullosa simplex Dowling-Meara due to an arginine to cysteine substitution in exon 1 of keratin 14 A Novel Mutation of KRT14 Gene in a Newborn with Epidermolysis Bullosa Simplex (Dowling-Meara Type): Case Report Keratin clumping in epidermolysis bullosa, Dowling-Meara type Epidermolysis bullosa simplex (Dowling-Meara type) associated with pyloric atresia and congenital urologic abnormalities A keratin K14 gene mutation in a Japanese patient with the Dowling-Meara type of epidermolysis bullosa simplex Epidermolysis bullosa simplex Dowling-Meara: Troublesome Blistering and Pruritus in an Adult Patient |