Abstract
Schimmelpenning Feuerstein Mims syndrome is a rare congenital hereditary syndrome characterized by the presence of one or more sebaceous nevi, structural and functional disorders of the visual, cardiovascular, bone and central nervous systems. The main marker of Schimmelpenning syndrome is the presence of sebaceous nevi on the skin of the face and neck a hamart of epidermal-follicular-sebaceous-apocrine origin. The aim of the article is to present our own clinical observation of Schimmelpenning Feuerstein Mims syndrome from the orphan diseases group. The syndrome is associated with a wide range of possible congenital pathologies, so such patients need timely interdisciplinary medical monitoring.
Publisher
Rossijskoe Obschestvo Dermatovenerologov i Kosmetologov
Subject
Infectious Diseases,Dermatology
Reference16 articles.
1. Diven DG, Solomon AR, McNeely MC, et al. Nevus sebaceous associated with major ophthalmologic abnormalities. Arch Dermatol 1987;123(3):383–386. doi: 10.101/archderm.1987.01660270121029
2. Тамразова О.Б., Заславский Д.В. Заболевания сальных желез у детей грудного возраста. Медицинский совет. 2019;2:152–160. [Tamrazova OB, Zaslavsky DV. Zabolevaniya sal'nyh zhelez u detey grudnogo vozrasta. Meditsinsky Sovet. 2019;2:152–160 (In Russ.)]
3. Горланов И.А., Леина Л.М., Милявская И.Р., Заславский Д.В. Детская дерматология. Руководство для врачей. ГЭОТАР-Медиа. М., 2022. 676 с. [Gorlanov IA, Leina LM, Milyavskaya IR, Zaslavsky DV. Detskaya dermatologiya. Rukovodstvo dlya vrachey. GEOTAR MEDIA. Moscow, 2022. 676 (In Russ.)]
4. Robert A Schwartz. Nevus Syndrome Clinical Presentation. 2021 Mar 23. In: Medscape [Internet].
5. Linear Nevus Sebaceous Syndrome: Case Reports and Review of the Literature