Devergie’s disease


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Abstract

The article provides data on a rare papulosquamous dermatosis, Devergie’s disease (DD). The incidence of DD is 1 in 5000 patients with new-onset skin disease. In recent years, an opinion about two types of this pathology has been expressed. The first begins after birth, in childhood or adolescence (child type); the second one occurs in adulthood (adult type). It is believed that the child type of DD is hereditary, and the adult is acquired. Based on the clinical picture, the age of the onset of the disease and the prognosis, six variants of the DD were identified. Treatment of dermatosis is carried out using both topical and systemic therapy, including genetic engineering biologic drugs.

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About the authors

Luiza A. Yusupova

Kazan State Medical Academy

Email: yuluizadoc@hotmail.com
Dr. Sci. (Med.), Professor, Head of the Department of Dermatovenereology and Cosmetology Kazan, Russia

Z. Sh Garaeva

Kazan State Medical Academy

Kazan, Russia

E. I Yunusova

Kazan State Medical Academy

Kazan, Russia

G. I Mavlyutova

Kazan State Medical Academy

Kazan, Russia

I. I Akhmetzyanova

Kazan State Medical Academy

Kazan, Russia

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