A case of junctional epidermolysis bullosa intermediate with collagen XVII deficiency treated with dupilumab

AbstractInherited epidermolysis bullosa is a heterogeneous group of hereditary skin diseases characterized by skin (mucosa) fragility, which leads to blistering. Junctional epidermolysis bullosa is associated with mutations in genes expressing proteins of the dermo-epidermal junction. Dupilumab, an...

Full description

Saved in:
Bibliographic Details
Main Authors: Li Zhang (Author), Shangshang Wang (Author), Qinyi Chen (Author), Leihong Xiang (Author)
Format: Book
Published: Taylor & Francis Group, 2023-12-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_e7d4b6bfd7e14cd2b02f4a1b7c70fea8
042 |a dc 
100 1 0 |a Li Zhang  |e author 
700 1 0 |a Shangshang Wang  |e author 
700 1 0 |a Qinyi Chen  |e author 
700 1 0 |a Leihong Xiang  |e author 
245 0 0 |a A case of junctional epidermolysis bullosa intermediate with collagen XVII deficiency treated with dupilumab 
260 |b Taylor & Francis Group,   |c 2023-12-01T00:00:00Z. 
500 |a 10.1080/09546634.2023.2253943 
500 |a 1471-1753 
500 |a 0954-6634 
520 |a AbstractInherited epidermolysis bullosa is a heterogeneous group of hereditary skin diseases characterized by skin (mucosa) fragility, which leads to blistering. Junctional epidermolysis bullosa is associated with mutations in genes expressing proteins of the dermo-epidermal junction. Dupilumab, an antibody that directly targets interleukin (IL)-4 receptor alpha, may be an effective treatment for dystrophic epidermolysis bullosa. We describe a case of junctional epidermolysis bullosa that improved with dupilumab. 
546 |a EN 
690 |a Junctional epidermolysis bullosa1 
690 |a dupilumab2 
690 |a treatment3 
690 |a COL17A14 
690 |a itch5 
690 |a pruritus6 
690 |a Dermatology 
690 |a RL1-803 
655 7 |a article  |2 local 
786 0 |n Journal of Dermatological Treatment, Vol 34, Iss 1 (2023) 
787 0 |n https://www.tandfonline.com/doi/10.1080/09546634.2023.2253943 
787 0 |n https://doaj.org/toc/0954-6634 
787 0 |n https://doaj.org/toc/1471-1753 
856 4 1 |u https://doaj.org/article/e7d4b6bfd7e14cd2b02f4a1b7c70fea8  |z Connect to this object online.