Cutaneous mosaicism, in KRT1 pI479T patient, caused by the somatic loss of the wild-type allele, leads to the increase in local severity of the disease
| Autor: | Gennaro Melino, Alessandro Terrinoni, E. Giannella, Margherita Annicchiarico-Petruzzelli, Biagio Didona, Ramona Palombo |
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| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
congenital hereditary and neonatal diseases and abnormalities Pathology medicine.medical_specialty Adolescent Hyperkeratosis Dermatology 030105 genetics & heredity medicine.disease_cause Severity of Illness Index Skin Diseases Meleda disease 030207 dermatology & venereal diseases 03 medical and health sciences 0302 clinical medicine Female Humans Keratin-1 Mutation Alleles Mosaicism otorhinolaryngologic diseases medicine Allele Ichthyosis business.industry Settore BIO/12 Wild type medicine.disease Phenotype Infectious Diseases Palmoplantar keratoderma business |
| Popis: | Background Epidermolytic ichthyosis (BCIE, OMIM 113800), is an autosomal dominant disorder of the skin caused by mutations in keratin genes KRT1 and KRT10. We present two sporadic patients showing a mild diffuse ichthyosis with palmoplantar keratoderma. Interestingly, one of them shows a significant hyperkeratosis of palms and soles similar to those present in the Meleda disease (OMIM 248300). Objective In this paper we would clarify the genetic difference between the two patients, giving rise to the different phenotype. Methods Clinical evaluation, followed by histological and molecular analysis has been established for these patients. Results We demonstrated the presence of a genetic cutaneous mosaicism. Both patients carry the KRT1 pI479T substitution, but in the palmoplantar areas of one of them, only the mutated allele is expressed (hemizygous). This leads to highlight a new type of cutaneous mosaic, the palmoplantar mosaicism. |
| Databáze: | OpenAIRE |
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