Keratitis, Ichthyosis, and Deafness Syndrome with Endocarditis and Myelitis: A Rare Case Report
<p>Introduction: Keratitis-ichthyosis-deafness (KID) syndrome (MIM#148210) is a rare autosomal dominant genodermatosis caused by monoallelic deleterious variants in the GJB2 gene (MIM*121011). The syndrome is characterized by congenital neurosensory deafness, keratitis, and palmoplantar k...
Guardat en:
| Autors principals: | , , , , , , |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Karger Publishers
2025-05-01
|
| Col·lecció: | Case Reports in Dermatology |
| Accés en línia: | https://karger.com/article/doi/10.1159/000546019 |
| Etiquetes: |
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|