Division of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
J Genet Couns. 2022 Dec;31(6):1434-1437. doi: 10.1002/jgc4.1616. Epub 2022 Aug 2.
Pathogenic variants in HPRT1 lead to deficiency in hypoxanthine-guanine phosphoribosyltransferase and are responsible for a spectrum of disorders. The severe phenotype is termed Lesch-Nyhan syndrome (LNS) and is inherited in an X-linked recessive manner. Most individuals with LNS have profound intellectual and physical disabilities throughout life including self-mutilating behaviors. Here, we present the case of a male infant who was diagnosed with LNS at 3 weeks of age via rapid exome sequencing (ES), which revealed a hemizygous maternally inherited deletion of at least 1.3 Mb of Xq26.3, including exons 2 to 9 of HPRT1. We discuss the critical time points leading to this diagnosis while highlighting his parents' values that guided the decision-making. Genetic testing provided an early diagnosis for this infant that led to important considerations regarding goals of care in addition to raising new ethical concerns. This highlights the important role that early and rapid diagnostic genetic testing can play in helping families make difficult decisions. Additionally, this case highlights the complexity of discussing rare genetic diagnoses with families and facilitating critical discussions to empower the family toward making an informed decision.
HPRT1 中的致病性变异导致次黄嘌呤-鸟嘌呤磷酸核糖基转移酶缺乏,从而导致一系列疾病。严重表型称为 Lesch-Nyhan 综合征(LNS),呈 X 连锁隐性遗传。大多数 LNS 患者一生都存在严重的智力和身体残疾,包括自残行为。在这里,我们介绍了一名男性婴儿的病例,他在 3 周大时通过快速外显子组测序(ES)被诊断为 LNS,该测序显示 Xq26.3 的至少 1.3 Mb 的单亲遗传缺失,包括 HPRT1 的外显子 2 至 9。我们讨论了导致这一诊断的关键时间点,同时强调了指导决策的父母价值观。遗传测试为这名婴儿提供了早期诊断,除了提出新的伦理问题外,还对护理目标进行了重要考虑。这突出了早期和快速诊断性遗传测试在帮助家庭做出困难决策方面的重要作用。此外,该病例还突出了与家庭讨论罕见遗传诊断的复杂性,并促进了关键讨论,以使家庭能够做出知情决策。