Clinical characteristics and management of clinically amyopathic juvenile dermatomyositis across four academic centers.

Bradley F., Bayer M. L., Co D. O., Chiu Y., Huber A. M., Ahmad R., ...Daha Fazla

Pediatric dermatology, cilt.38, sa.2, ss.413-419, 2021 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 38 Sayı: 2
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1111/pde.14510
  • Dergi Adı: Pediatric dermatology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, CAB Abstracts, EMBASE, MEDLINE
  • Sayfa Sayıları: ss.413-419
  • Marmara Üniversitesi Adresli: Hayır

Özet

Background/Objectives: Clinically amyopathic juvenile dermatomyositis (CAJDM) is an uncommon but important subset of patients with juvenile dermatomyositis, characterized by pathognomonic cutaneous findings without clinically evident muscle weakness. With limited data available and lack of standardized management guidelines for CAJDM, we sought to describe common features, including early indicators that may be associated with progression of muscle disease, and review the course and treatment of these patients.