A de novo mutation of KRT1 in a baby girl causing epidermolytic ichthyosis with impressive epidermolytic palmoplantar keratoderma.
Dermatol Online J
; 26(7)2020 Jul 15.
Article
en En
| MEDLINE
| ID: mdl-32898404
We report a 6-year-old girl showing epidermolytic ichthyosis/epidermolytic hyperkeratosis (EI/EH). Targeted Next Generation Sequencing revealed a de novo, previously unidentified KRT1 mutation. The findings of this study expands the clinical and spectrum and genotype-phenotype correlation associated with EI/EH.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Hiperqueratosis Epidermolítica
/
Queratodermia Palmoplantar Epidermolítica
/
Queratina-1
/
Mutación
Límite:
Child
/
Female
/
Humans
Idioma:
En
Revista:
Dermatol Online J
Asunto de la revista:
DERMATOLOGIA
Año:
2020
Tipo del documento:
Article