Sažetak sa skupa
https://doi.org/10.26800/LV-144-supl2-CR77
Juvenile dermatomyositis with vasculopathy
Mia Kovačević
; School of Medicine University of Zagreb
Magdalena Kujundžić
; School of Medicine University of Zagreb
Marijana Frković
; Division for Pediatric Rheumatology, Department of Pediatrics; University Hospital Centre ZagrebSchool of Medicine University of Zagreb
Sažetak
Juvenile dermatomyositis (JDM) is rare, but serious disease with many possible complications. Hallmarks of this disease are heliotrope erythema, periorbital edema and Gottrone papules combined with symmetric proximal muscle weakness that usually slowly progresses over period of weeks and months. In most cases the age of onset is between 4 and 10 years. There are four subtypes of the disease with variable course, organ involvement
and long-term clinical outcome.
Ključne riječi
Infliximab, juvenile dermatomyositis, vascu- lopathy
Hrčak ID:
279893
URI
Datum izdavanja:
27.4.2022.
Posjeta: 453 *