Orphanic diseases: Schimmelpenning — Feuerstein — Mims syndrome
D. V. ZaslavskySaint Petersburg State Pediatric Medical UniversityA. A. SydikovFergana Medical Institute of Public HealthEkaterina V. GrekovaI.M. Sechenov First Moscow State Medical UniversityМарат Риатович ГафиатулинSaint Petersburg State Pediatric Medical UniversityKseniya A. KovalenkoSaint Petersburg State Pediatric Medical UniversityЕ.А. БогдановаSaint Petersburg State Pediatric Medical UniversityNatalya A. BerezkinaSaint Petersburg State Pediatric Medical University
ABI
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.
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