A Case with Netherton Syndrome-Classical Findings in Late Diagnosis

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VEZİR E., Nural Kirci E. G., Özcan A.

Asthma Allergy Immunology, cilt.20, sa.1, ss.64-67, 2022 (Scopus, TRDizin)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 20 Sayı: 1
  • Basım Tarihi: 2022
  • Doi Numarası: 10.21911/aai.635
  • Dergi Adı: Asthma Allergy Immunology
  • Derginin Tarandığı İndeksler: Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.64-67
  • Anahtar Kelimeler: Anaphylaxis, hypereosinophilia, hyper-IgE, ichthyosis, multiple food allergy, netherton syndrome
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Sağlık Bilimleri Üniversitesi Adresli: Evet

Özet

Netherton syndrome is a rare disease with autosomal recessive inheritance and characterized by the triad of congenital ichthyosiform erytroderma, trichorrhexis invaginata, and atopic manifestations. We herein report a patient who presented to the pediatric allergy and clinical immunology outpatient clinic with signs of ichthyosis, multiple food allergy, anaphylaxis, hypereosinophilia, and hyperimmunoglobulinemia E (hyper-IgE), and was diagnosed as having Netherton syndrome.