Tetrasomy 21 pter→q21.3 due to an extra +dic(21;21)mat in a severely psychomotor-retarded female patient without Down syndrome phenotype

• Published in: European journal of medical genetics 2020-04, Vol.63 (4), p.103824-103824, Article 103824
• Main Authors: Takano, Takako, Nakabayashi, Kazuhiko, Ota, Hideomi, Arai, Yasuhiro, Kamura, Hiromi, Hata, Kenichiro
• Format: Article
• Language: English
• Subjects: Abnormalities, Multiple - genetics; Breakage-fusion-bridge cycles; Child; Chromosome 21; Chromosomes, Human, Pair 21 - genetics; Cleft Lip - genetics; Cleft Palate - genetics; Female; Humans; In Situ Hybridization, Fluorescence; Intellectual Disability - genetics; Karyotype; Karyotyping; Microcephaly - genetics; Phenotype; Psychomotor retardation; Tetrasomy; Tetrasomy 21; Whole Genome Sequencing
• ISSN: 1769-7212; 1878-0849
• DOI: 10.1016/j.ejmg.2019.103824

Complete or partial tetrasomy 21 has been reported only in rare cases. We report a Japanese female patient with tetrasomy 21 due to an extra chromosome derived from chromosome 21 (Chr21). The patient had severe psychomotor retardation without Down syndrome (DS) phenotype; she showed short stature, microcephaly, round face, cleft lip and palate, and other dysmorphic features. The chromosome analyses for the patient detected an extra dicentric Chr21 consisting of two partial Chr21 copies fused together within their long arms. Her karyotype was revealed to be 47,XX,+dic(21;21). Allelic ratios of heterozygous SNPs observed in the patient indicated the maternal origin of the extra Chr21. Copy number and structural variant analyses using whole genome sequencing data indicated that the distal breakpoint of the dicentric Chr21 was located within 21q21.3 and that the extra Chr21 did not simply consist of inverted duplications of the pter→q21.3 region, but likely contained multiple partial deletions, duplications, and inversions within it. Fluorescence in situ hybridization results were consistent with the karyotype and genomic analyses. The patient's lack of DS phenotype turned out to be due to the normal copy number of the DS critical region (21q22.13–22.3). A possible molecular mechanism leading to the complex genomic rearrangements in the tetrasomic region consists mainly of breakage-fusion-bridge cycles with an unequal crossing-over event.