A case report of harlequin ichthyosis with a favorable outcome: Early treatment and significant recovery
Harlequin ichthyosis is the most severe form of autosomal-recessive congenital ichthyoses with a high mortality rate. In affected infants, mutations occur in the ABCA12 gene. The ABCA12 gene produces the proteins that are essential for the natural development of skin cells. In this disease, disrupti...
| Main Authors: | , , |
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| Format: | Article |
| Language: | fas |
| Published: |
Tehran University of Medical Sciences
2019-01-01
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| Series: | حیات |
| Subjects: | |
| Online Access: | http://hayat.tums.ac.ir/article-1-2377-en.html |