Hereditary Hyperferritinemia Cataract Syndrome: Case Report

Guzelkucuk Z., ÇAKMAKLI H. F., Onen M., Pietrangelo A., Yarali N.

GAZI MEDICAL JOURNAL, cilt.31, sa.3, ss.445-446, 2020 (ESCI, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 31 Sayı: 3
  • Basım Tarihi: 2020
  • Doi Numarası: 10.12996/gmj.2020.108
  • Dergi Adı: GAZI MEDICAL JOURNAL
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, Academic Search Premier
  • Sayfa Sayıları: ss.445-446
  • Anahtar Kelimeler: Hyperferritinemia, cataract, L-Ferritin
  • Ankara Üniversitesi Adresli: Evet

Özet

Hereditary Hyperferritinemia-Cataract Syndrome (HHCS) is a rare disease characterized by cataract and hyperferritinemia. Herein, we present a pediatric patient diagnosed with HHCS.