Caricamento...
Congenital ichthyosiform erythroderma with a novel variant in ABCA12 in a Chinese patient
INTRODUCTION: Congenital ichthyosiform erythroderma (CIE ) is characterized by fine, whitish scales on a background of erythematous skin over the whole body; it is reportedly caused by mutations in ABCA12, ALOX12B, ALOXE3, CERS3, CYP4F22, NIPAL4, PNPLA1, and TGM1 genes. CASE PRESENTATION: A 15‐month...
Salvato in:
| Pubblicato in: | Pediatr Investig |
|---|---|
| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2020
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7331307/ https://ncbi.nlm.nih.gov/pubmed/32851342 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ped4.12182 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|