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akaturk Akademik ölçüm

Makale detayı · 2025

Evaluation of the Relationship Between Neurologic Manifestations and Genetic Mutations in Wilson’s Disease with Next-Generation Sequencing

Diagnostics

YÖKSİS OpenAlex Açık erişim · gold SJR Q2 JCR Q1 Atıf 3 Yüzdelik 83.2% FWCI 1.59
Yıl
2025
ISSN
2075-4418
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

Background: Wilson’s disease (WD) is a rare autosomal recessive disorder caused by mutations in the ATP7B gene, leading to copper accumulation in the liver and brain. Given the clinical heterogeneity of the disease, this study aimed to characterize the mutational spectrum of ATP7B and explore genotype–phenotype correlations in Turkish patients. Methods: Whole-exome sequencing (WES) was performed in 17 Turkish patients clinically diagnosed with WD. Variants were annotated and evaluated using five in silico prediction tools (REVEL, CADD, PolyPhen, SIFT, MutationTaster). Copy number variation (CNV) analysis was conducted using the CLC Genomics Server (Version 22.0.2). Results: A total of 14 distinct ATP7B variants were identified, comprising 12 missense, 1 nonsense, and 1 frameshift mutation. Variant distribution showed some phenotype-specific patterns: four variants were found more frequently in hepatic cases and three in neurological cases, although no statistically significant or consistent correlation between genotype and clinical presentation could be established. The most frequent mutation was p.His1069Gln, present in both phenotypes. All missense variants were predicted to be pathogenic by at least three computational tools, with high concordance among platforms. No pathogenic CNVs were detected. Conclusions: This study expands the mutational landscape of ATP7B in Turkish patients with WD and supports the utility of WES combined with in silico tools for accurate variant classification. The results emphasize the genetic heterogeneity of WD and suggest possible associations between certain mutations and clinical phenotypes.

Konular

  • Trace Elements in Health
  • Heavy Metal Exposure and Toxicity
  • Aluminum toxicity and tolerance in plants and animals

Birincil konu Trace Elements in Health

Yazarlar

  1. AHMET SAMİ AKBULUT İNÖNÜ ÜNİVERSİTESİ
  2. ŞEYMA İŞ
  3. TUĞBA KUL KÖPRÜLÜ
  4. FATMA İLKNUR VAROL
  5. ZEYNEP KÜÇÜKAKÇALI
  6. CEMİL ÇOLAK İNÖNÜ ÜNİVERSİTESİ
  7. AHMET KOÇ
  8. ŞABAN TEKİN
  9. SEZAİ YILMAZ