Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing. (3rd February 2022)

• Record Type: Journal Article
• Authors: Yahia, Ashraf; Ayed, Ikhlas Ben; Hamed, Ahlam A.; Mohammed, Inaam N.; Elseed, Maha A.; Bakhiet, Aisha M.; Guillot‐Noel, Lena; Abozar, Fatima; Adil, Rawaa; Emad, Sara; Abubaker, Rayan; Musallam, Mhammed Alhassan; Eltazi, Isra Z. M.; Omer, Zulfa; Maaroof, Omer M.; Soussi, Amal; Bouzid, Amal; Kmiha, Sana; Kamoun, Hassen; Salih, Mustafa A.; Ahmed, Ammar E.; Elsayed, Liena; Masmoudi, Saber; Stevanin, Giovanni
• Is Part Of: Annals of human genetics. Volume 86:Number 4(2022)
• Page Start: 181
• Page End: 194
• Publication Date: 2022-02-03
• Subjects: ADAT3 -- ATP2B3 -- CCDC82 -- HERC2 -- HUWE1 -- syndromic intellectual disability; Human genetics -- Periodicals; 599.935
• DOI: 10.1111/ahg.12460
• Languages: English
• ISSNs: 0003-4800

Abstract

Abstract: Background: Intellectual disability is a form of neurodevelopmental disorders that begin in childhood and is characterized by substantial intellectual difficulties as well as difficulties in conceptual, social, and practical areas of living. Several genetic and nongenetic factors contribute to its development; however, its most severe forms are generally attributed to single‐gene defects. High‐throughput technologies and data sharing contributed to the diagnosis of hundreds of single‐gene intellectual disability subtypes. Method: We applied exome sequencing to identify potential variants causing syndromic intellectual disability in six Sudanese patients from four unrelated families. Data sharing through the Varsome portal corroborated the diagnosis of one of these patients and a Tunisian patient investigated through exome sequencing. Sanger sequencing validated the identified variants and their segregation with the phenotypes in the five studied families. Result: We identified three pathogenic/likely pathogenic variants in CCDC82, ADAT3, and HUWE1 and variants of uncertain significance in HERC2 and ATP2B3 . The patients with the CCDC82 variants had microcephaly and spasticity, two signs absent in the two previously reported families with CCDC82 ‐related intellectual disability. Conclusion: In conclusion, we report new patients with pathogenic mutations in the genes CCDC82, ADAT3, and HUWE1 . We also highlight the possibility of extending the CCDC82 ‐linked phenotype to include spastic paraplegia and microcephaly.