Extensive Extragenital Lichen Sclerosus-Like Lesions in a Patient with Junctional Epidermolysis Bullosa
Epidermolysis bullosa (EB) is a heterogeneous group of genetic disorders characterized by the formation of blisters either spontaneously or at the sites of trauma. These heal with post-inflammatory hypopigmentation, scarring, or milia formation. We hereby present a child who presented with widesprea...
Saved in:
Main Authors: | Smriti Gupta (Author), Sanjeev Handa (Author), Debajyoti Chatterjee (Author), Dipankar De (Author), Rahul Mahajan (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2024-08-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Extragenital lichen sclerosus with angiokeratoma-like changes
by: Gabriela F. Melo, et al.
Published: (2022) -
An unusual presentation of extragenital lichen sclerosus-An extensive keratotic variant
by: Mario Magaña, et al.
Published: (2024) -
Topical gentamicin 0.1% promotes collagen 7 expression in recessive dystrophic epidermolysis bullosa
by: Rahul Mahajan, et al.
Published: (2022) -
Dermoscopic evaluation of extragenital lichen sclerosus et atrophicus
by: Sunanda Arun Mahajan, et al.
Published: (2022) -
Dermoscopic findings in extragenital lichen sclerosus
by: Anna Jędrowiak, et al.
Published: (2018)