Interstitial microdeletions of 3q26.2q26.31 in two patients with neurodevelopmental delay and distinctive features. Issue 2 (7th November 2022)

• Record Type: Journal Article
• Authors: Tamura, Takeaki; Yamamoto Shimojima, Keiko; Shiihara, Takashi; Sakazume, Satoru; Okamoto, Nobuhiko; Yagasaki, Hiroshi; Morioka, Ichiro; Kanno, Hitoshi; Yamamoto, Toshiyuki
• Is Part Of: American journal of medical genetics. Volume 191:Issue 2(2023)
• Page Start: 400
• Page End: 407
• Publication Date: 2022-11-07
• Subjects: 3q26.2q26.31 deletion -- congenital heart defects -- FNDC3B -- neurodevelopmental delays -- NLGN1 -- PLD1; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.63034
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract: Interstitial microdeletions in the long arm of chromosome 3 are rare. In this study, we identified two patients with approximately 5‐Mb overlapping deletions in the 3q26.2q26.31 region. Both patients showed neurodevelopmental delays, congenital heart defects, and distinctive facial features. One of them showed growth deficiency and brain abnormalities, as shown on a magnetic resonance imaging scan. Haploinsufficiency of NLGN1 and FNDC3B present in the common deletion region was considered to be responsible for neurodevelopmental delay and the distinctive features, respectively. The possibility of unmasked variants in PLD1 was considered and analyzed, but no possible pathogenic variant was found, and the mechanism of the congenital heart defects observed in the patients is unknown. Because 3q26.2q26.31 deletions are rare, more information is required to establish genotype–phenotype correlations associated with microdeletions in this region.