Neurofibromatosis Type 1 in Children: A Single-Center Experience

Kacar A. G., KILINÇ OKTAY B., Ozel S., OCAK S., GÜNEŞ N., ULUDAĞ ALKAYA D., ...Daha Fazla

TURKISH ARCHIVES OF PEDIATRICS, cilt.56, sa.4, ss.339-343, 2021 (ESCI, Scopus, TRDizin) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 56 Sayı: 4
  • Basım Tarihi: 2021
  • Doi Numarası: 10.5152/turkarchpediatr.2021.20165
  • Dergi Adı: TURKISH ARCHIVES OF PEDIATRICS
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.339-343
  • İstanbul Üniversitesi-Cerrahpaşa Adresli: Evet

Özet

Objective: Neurofibromatosis (NF) is the most common autosomal dominantly inherited neurocutaneous syndrome. The characteristic features of NF type 1 (NF-1) are cafe au lait spots, axillary and inguinal freckling, peripheral neurofibromas, optic pathway glioma, and Lisch nodules. The present study aimed to analyze the clinical features of children with NF-1.