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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Autors principals: Nailya R. Pimenova (Autor), Elena I. Kashirskaya (Autor), Anastasiya V. Alekseeva (Autor)
Format: Llibre
Publicat: Union of pediatricians of Russia, 2023-08-01T00:00:00Z.
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