Clinical observation of familial cases of congenital ichthyosis
Background. Ichthyosis is a group of rare genetic diseases with a wide phenotypic spectrum, characterized most often by generalized hyperkeratinization and desquamation with variable erythema [1]. In most cases, the diagnosis is established immediately after birth on the basis of clinical data. The...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
Union of pediatricians of Russia
2023-08-01
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| Series: | Педиатрическая фармакология |
| Subjects: | |
| Online Access: | https://www.pedpharma.ru/jour/article/view/2344 |
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