Tuberous sclerosis syndrome: a typical case of a rare disease

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The article is devoted to a rare hereditary disease from the group of phak omatoses with an autosomal dominant type of inheritance — Pringle — Burnevill disease. The questions of the prevalence of the disease, the variability of the clinical picture, the timeliness of the clinical diagnosis are considered. Particular attention is paid to skin manifestations and their differential diagnosis. A clinical case of this disease is described.

About the authors

V. A. Okhlopkov

Omsk State Medical University


Dr. Sci. (Med.), Prof., Departmental Head, Department of Dermatovenereology and Cosmetology

Lenina str., 12, Omsk, 644099, Russian Federation

Russian Federation

E. A. Zykova

Omsk State Medical University

Author for correspondence.

Cand. Sci. (Med.), Assistant, Department of Dermatovenereology and Cosmetology

Lenina str., 12, Omsk, 644099, Russian Federation

Russian Federation

O. V. Pravdina

Omsk State Medical University


Cand. Sci. (Med.), Assoc. Prof., Department of Dermatovenereology and Cosmetology

Lenina str., 12, Omsk, 644099, Russian Federation

Russian Federation


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Copyright (c) 2018 Okhlopkov V.A., Zykova E.A., Pravdina O.V.

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