A Rare Syndrome Leading to Immunodeficiency: Zhu-Tokita-Takenouchi-Kim Syndrome İmmün Yetmezliğe Yol Açan Nadir Bir Sendrom: Zhu-Tokita-Takenouchi-Kim Sendromu

ÖZKAN G., KILIÇ GÜLTEKİN S. Ş.

Turkiye Klinikleri Pediatri, cilt.33, sa.2, ss.76-80, 2024 (Scopus) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 33 Sayı: 2
  • Basım Tarihi: 2024
  • Doi Numarası: 10.5336/pediatr.2024-101224
  • Dergi Adı: Turkiye Klinikleri Pediatri
  • Derginin Tarandığı İndeksler: Scopus, Academic Search Premier, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.76-80
  • Anahtar Kelimeler: genetics, Immune deficiency disease
  • Bursa Uludağ Üniversitesi Adresli: Evet

Özet

Zhu-Tokita-Takenouchi-Kim (ZTTK) syndrome, a rare autosomal dominant genetic disease, is caused by a loss-of-function mutation in the SON gene, first described in 2015. The clinical features of the disease are dysmorphic craniofacial appearance, hypotonia, brain malformations, intellectual disability, musculoskeletal abnormalities, and congenital heart and genito-urinary system defects. The literature about ZTTK syndrome is limited, and the majority of them focus on clinical and genetic findings. Here, we present an immunocompromised patient with ZTTK syndrome due to a de novo mutation in the SON gene. There are no published data about the detailed immunologic parameters of ZTTK syndrome.