Langman Craig B, Delos Santos Rowena B, Ghossein Cybele, Atherton Andrea M, Levtchenko Elena N, Servais Aude
Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Washington University in St Louis, St Louis, Missouri, USA.
Kidney Int Rep. 2023 Nov 3;9(2):214-224. doi: 10.1016/j.ekir.2023.10.030. eCollection 2024 Feb.
Cystinosis is a rare, inherited, lysosomal storage disorder characterized by the progressive accumulation of intralysosomal cystine and subsequent organ and tissue damage. The kidneys are the first and most severely impacted organ. Although cystinosis was once considered a fatal pediatric disease, patients with cystinosis are living well into adulthood with advances in medical care, including kidney transplant and early and continuous use of cysteamine therapy. This increase in life expectancy has revealed an extrarenal phenotype of cystinosis that emerges in adolescence and adulthood, affecting nearly all body systems, including the endocrine and reproductive systems. As individuals with cystinosis are planning for the future, reproductive health and fertility have become areas of increased focus. This narrative review aims to summarize the current understanding of reproductive health and fertility in patients with cystinosis and discuss practical considerations for monitoring and managing these complications.
胱氨酸贮积症是一种罕见的遗传性溶酶体贮积病,其特征是溶酶体内胱氨酸进行性蓄积,随后导致器官和组织损伤。肾脏是首个且受影响最严重的器官。尽管胱氨酸贮积症曾被认为是一种致命的儿科疾病,但随着医疗护理的进步,包括肾移植以及早期持续使用半胱胺治疗,患有胱氨酸贮积症的患者能够活到成年。预期寿命的延长揭示了胱氨酸贮积症在青少年和成年期出现的肾外表型,几乎影响所有身体系统,包括内分泌和生殖系统。随着患有胱氨酸贮积症的个体为未来做规划,生殖健康和生育能力已成为日益关注的领域。这篇叙述性综述旨在总结目前对胱氨酸贮积症患者生殖健康和生育能力的认识,并讨论监测和管理这些并发症的实际考虑因素。