Hereditary palmoplantar keratoderma. Two clinical cases

Rodin A.Yu.

Volgograd State Medical University, Department of Dermatovenereology, Volgograd, Russia

A literature review of the pathogenesis, classification, clinical manifestations, diagnostics and treatment principles of hereditary palmoplantar keratoderma is conducted. Two clinical cases are presented. The first case is a 3-year-old girl and her mother with diffuse palmoplantar keratoderma type Unna-Thost (according to the patients words, similar lesions were found in the eldest daughter and grandfather). The second case is a 67-year-old patient with punctate palmoplantar keratoderma (Buschke-Fischer syndrome) in combination with bilateral cataracts and moderate neuropsychiatric disorders.

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About the Authors

Aleksey Yu. Rodin, Dr. Sci. (Med.), Professor, Professor at the Department of Dermatovenereology, Volgograd State Medical University, Volgograd, Russia; dermavolgmu@yandex.ru, eLibrary SPIN:7963-3380, ORCID: https://orcid.org/0000-0003-1630-5880

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