| Autor: |
K S Chandan, S R Ashitha, Sachin Somashekhar, L Shishira |
| Jazyk: |
angličtina |
| Rok vydání: |
2020 |
| Předmět: |
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| Zdroj: |
Indian Journal of Paediatric Dermatology, Vol 21, Iss 3, Pp 221-223 (2020) |
| Druh dokumentu: |
article |
| ISSN: |
2319-7250 |
| DOI: |
10.4103/ijpd.IJPD_102_19 |
| Popis: |
Epidermolytic ichthyosis (EI) previously named bullous congenital ichthyosiform erythroderma of Brocq or epidermolytic hyperkeratosis (mostly considered as a histological term now) is rare with a variable defect of cornification, clinically characterized by generalized erythema, erosions, scaling, and easily breaking blisters that become less frequent later in life while hyperkeratosis increases. It is usually inherited in an autosomal-dominant fashion and is caused by the mutations in the genes KRT1 and KRT10, coding for the proteins keratin 1 and keratin 10, respectively. To date, only six recessive KRT10 mutations have been shown to cause autosomal-recessive EI, all of which have been found to lead to the complete absence of the keratin 10 protein. To the best of our knowledge, this is the first such case report from India. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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