Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Am J Med Genet A. 2023 Jul;191(7):1978-1983. doi: 10.1002/ajmg.a.63224. Epub 2023 May 3.
Uniparental disomy (UPD) is the inheritance of both chromosomal homologs from one parent. Depending on the chromosome involved and the parental origin, UPD may result in phenotypic abnormalities due to aberrant methylation patterns or unmasking recessive conditions in isodisomic regions. UPD primarily originates from somatic rescue of a single meiotically-derived aneuploidy, most commonly a trisomy. Double UPD is exceedingly rare and triple UPD has not been previously described. Here, we report two unrelated clinical cases with UPD of multiple chromosomes; an 8-month-old male with maternal isodisomy of chromosome 7 and paternal isodisomy of chromosome 9, and a 4-week-old female with mixed paternal UPD for chromosomes 4, 10, and 14. These cases also demonstrate that although extremely rare, the detection of AOH on two or more chromosomes may warrant additional clinical and laboratory investigation such as methylation and STR marker analysis, especially when involving chromosomes known to be associated with imprinting disorders.
单亲二倍体 (UPD) 是指从一个亲本遗传两个染色体同源物。根据涉及的染色体和亲本来源,UPD 可能由于异常甲基化模式或使同二倍体区域中的隐性条件显现而导致表型异常。UPD 主要源于单个减数分裂衍生的非整倍体的体细胞拯救,最常见的是三体。双 UPD 极为罕见,三重 UPD 以前尚未描述过。在这里,我们报告了两个无关的临床病例,涉及多个染色体的 UPD;一个 8 个月大的男性,其母亲的 7 号染色体和父亲的 9 号染色体为同二倍体,一个 4 周大的女性,其父亲的 4 号、10 号和 14 号染色体为混合 UPD。这些病例还表明,尽管极其罕见,但在两个或更多染色体上检测到 AOH 可能需要进行额外的临床和实验室检查,例如甲基化和 STR 标记分析,尤其是当涉及已知与印迹障碍相关的染色体时。