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Browse result for Bullous ichthyosiform erythroderma
※ introduction Epidermolytic ichthyosis (EI), is a severe form of dry scaly skin, that initially presents with redness, blisters, erosions, and peeling in a newborn baby. Hyperkeratosis typically develops several months later. Other symptoms include itch, painful fissures, strong body odor, and absence of sweat. Symptoms vary in severity and extent of skin involvement. The two main types are divided into one involving palms and soles and the other without.
EI is caused by a genetic mutation. The condition involves the clumping of keratin filaments.
The condition is rare, affecting around 1 in 200,000 to 300,000 babies.
Reference
Wiki: Bullous ichthyosiform erythroderma
Reference
Wiki: Bullous ichthyosiform erythroderma
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD03719 | P04264 | 3848 | KRT1 | Keratin, type II cytoskeletal 1 | Homo sapiens |
| PTMD04151 | P13645 | 3858 | KRT10 | Keratin, type I cytoskeletal 10 | Homo sapiens |
