Pretibial dystrophic epidermolysis bullosa pruriginosa: A rare case report in a child with low intelligent quotient
Dystrophic epidermolysis bullosa (DEB), a rare form of EB, is characterized by defects in Type VII collagen which is encoded by COL7A1 gene located on chromosome 3p21. A 12-year-old female with low intelligent quotient presented with intensely pruritic multiple violaceous papules which were coalesce...
Saved in:
Main Authors: | B Vijaya (Author), S R Narahari (Author), Pallavi Deka (Author), G V Manjunath (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2016-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Pretibial dystrophic epidermolysis bullosa
by: Elisabeth de Albuquerque Cavalcanti Callegaro, et al.
Published: (2017) -
A newborn with dystrophic epidermolysis bullosa, self-improving and mother with epidermolysis bullosa pruriginosa
by: Yi-Chen Huang, et al.
Published: (2023) -
Dominant Dystrophic Epidermolysis Bullosa Pruriginosa Responding to Naltrexone Treatment
by: Kristine A.U. Pallesen, et al.
Published: (2019) -
Pretibial Epidermolysis Bullosa
by: Joshi Arun, et al.
Published: (2002) -
Epidermolysis bullosa pruriginosa
by: Puri Suruchi, et al.
Published: (2005)