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Article detail · 2023

Clinical exome sequencing reveals an important role for clinical diagnosis of intellectual disability with definition of seven novel variants

Neurology Asia

YÖKSİS OpenAlex Open access · bronze SJR Q4 JCR Q4 Citations 2 Percentile 70.7% FWCI 0.43
Year
2023
ISSN
1823-6138
Type
article

Data source split

  • YÖKSİS YÖKSİS article record
  • OpenAlex OpenAlex enrichment (abstract, citations, topics)

Abstract

English (OpenAlex)

Intellectual disability can be defined as a significantly below-average general mental function, accompanied by environmental adaptation and behavioural deterioration. Patient files of 87 children with intellectual disability were evaluated in this study. After clinical exclusion criterias, clinical exome sequencing was performed for 25 of 87 intellectual disability cases with a massively parallel targeted sequencing method. Seventeen variants in the genes MBOAT7, KDM5C, TUBB3, MAN1B1, GFAP, CACNA1A, BCOR, LMNA, LBR, ALS2, ENPP1, UBE3A, TRAPPC9, HSPG2, AFF2, NLGN4, and SOX10 were identified in 14 of 25 patients (56%). Seven of the 17 variants (41.1%) were novel in the genes KDM5C, BCOR, UBE3A, TRAPPC9, AFF2, NLGN4, and SOX10. Seven cases (7/25, 28%) had a definite diagnosis of intellectual disability with their pathogenic variants. The high rate of variant detection (56%) in the current study shows that multiple gene analysis plays an essential role in diagnosing the uncertain etiology of intellectual disability. This study also presents seven novel variants, which are first reported.

Topics

  • Genomics and Rare Diseases
  • Genetics and Neurodevelopmental Disorders
  • Genomic variations and chromosomal abnormalities

Primary topic Genomics and Rare Diseases

Authors

  1. SİNEM YALÇINTEPE
  2. IŞIK GÖRKER TRAKYA ÜNİVERSİTESİ
  3. LEYLA BOZATLI TRAKYA ÜNİVERSİTESİ
  4. Hazal Sezginer Gürel
  5. DRENUSHE ZHURI IPCI
  6. SELMA DEMİR
  7. EMİNE İKBAL ATLI
  8. ENGİN ATLI
  9. DAMLA EKER
  10. HAKAN GÜRKAN