Du Yufang, Liao Liangrong, Wei Xianda, Ma Yunting, Shi Meizhen, Li Chunyan, Liu Juliang, Lin Wenting, Zeng Hao, Chen Shaoke, Gui Baoheng
Center for Medical Genetics and Genomics, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
The Guangxi Health Commission Key Laboratory of Medical Genetics and Genomics, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Genet Res (Camb). 2025 Jul 21;2025:1368153. doi: 10.1155/genr/1368153. eCollection 2025.
49, XXXYY is a rare form of sex chromosomal aneuploidy that has been reported in 11 cases worldwide. The parental origin of the extra sex chromosomes and the specific clinical features of this condition remain unclear. We recruited a case with 49, XXXYY and performed genome-wide copy number variation analysis using next-generation sequencing. In addition, the parental origin of the extra sex chromosomes was determined through short tandem repeats (STRs) locus genotyping. Furthermore, a comprehensive review and comparison of clinical phenotypes were conducted among 12 cases with 49, XXXYY. The patient exhibited a karyotype of 49, XXXYY without any mosaic patterns. No pathogenic microdeletions or microduplications (> 100 kb) were identified in autosomes 1-22. Analysis of the STR loci revealed that two of three X chromosomes originated from father. This suggests that the nondisjunction of chromosomes X and Y during stages I and II of meiotic spermatogenesis led to the production of an abnormal sperm with XXYY. Subsequently, fertilization of a normal oocyte with this abnormal sperm resulted in an abnormal zygote with pentasomy XXXYY. The main clinical features observed in these cases included varying degrees of mental retardation, minor facial dysmorphology, and gonadal or endocrine abnormalities. In conclusion, 49, XXXYY is a rare chromosomal disorder characterized by mental retardation and facial dysmorphology. Nondisjunction of chromosomes X and Y during stages I and II of meiotic spermatogenesis is a critical factor contributing to the development of this abnormal karyotype.
49, XXXYY是一种罕见的性染色体非整倍体形式,全球已报道11例。额外性染色体的亲本来源以及该病症的具体临床特征仍不清楚。我们招募了一名49, XXXYY患者,并使用下一代测序进行全基因组拷贝数变异分析。此外,通过短串联重复序列(STRs)位点基因分型确定了额外性染色体的亲本来源。此外,还对12例49, XXXYY患者的临床表型进行了全面回顾和比较。该患者表现出49, XXXYY核型,无任何嵌合模式。在1 - 22号常染色体中未发现致病性微缺失或微重复(> 100 kb)。STR位点分析显示三条X染色体中有两条来自父亲。这表明减数分裂精子发生的I期和II期期间X和Y染色体的不分离导致产生了具有XXYY的异常精子。随后,该异常精子与正常卵母细胞受精导致形成具有五体性XXXYY的异常合子。这些病例中观察到的主要临床特征包括不同程度的智力迟钝、轻微面部畸形以及性腺或内分泌异常。总之,49, XXXYY是一种以智力迟钝和面部畸形为特征的罕见染色体疾病。减数分裂精子发生的I期和II期期间X和Y染色体的不分离是导致这种异常核型形成的关键因素。