{"id":11727,"date":"2025-07-26T04:29:18","date_gmt":"2025-07-26T02:29:18","guid":{"rendered":"https:\/\/valintermed.com\/?p=11727"},"modified":"2025-07-26T04:29:18","modified_gmt":"2025-07-26T02:29:18","slug":"ihtioz-obyknovennyy","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/obyknovennyy-ihtioz\/","title":{"rendered":"Ichthyosis vulgaris"},"content":{"rendered":"
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Ichthyosis vulgaris (or ichthyosis) is a group of hereditary or acquired diseases characterized by a disruption of the normal function of skin keratinization. The main manifestation of this disease is hyperkeratosis, which leads to an increase in the thickness of the stratum corneum of the skin and the formation of scaly spots. According to clinical manifestations, ichthyosis can be different: from mild dryness and flaking to more severe forms with a pronounced inflammatory reaction, itching and even infectious complications. The disease can manifest itself as an independent pathology or as part of syndromes, which makes it diverse in its clinical picture. Ichthyosis vulgaris is of particular importance in the field of dermatovenereology and genetics, since it requires a multidisciplinary approach to diagnosis and treatment.<\/p>\n

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