Suppr超能文献

患有戈谢病的女性。

Women with Gaucher Disease.

作者信息

Meijon-Ortigueira Maria Del Mar, Solares Isabel, Muñoz-Delgado Cecilia, Stanescu Sinziana, Morado Marta, Pascual-Izquierdo Cristina, Villalon Blanco Lucía, Belanger Quintana Amaya, Menéndez-Conde Covadonga Pérez, Morales-Conejo Montserrat, Villarrubia-Espinosa Jesús

机构信息

Department of Hematology, Hospital Universitario Ramón y Cajal-IRYCIS, 28034 Madrid, Spain.

Department of Internal Medicine, Clínica Universidad de Navarra, 28027 Madrid, Spain.

出版信息

Biomedicines. 2024 Mar 5;12(3):579. doi: 10.3390/biomedicines12030579.

Abstract

Gaucher disease is an inherited disorder in which there is a deficiency of the enzyme glucocerebrosidase, which leads to the accumulation of glucosylceramide. Although much scientific evidence is now available, there is still limited data on the impact on the different life stages of women with this disease. Among other alterations, a delay in menarche has been described, although it has not been related to fertility problems. Menorrhagia is relatively frequent, being related to the presence of thrombocytopenia, thrombocytopathies or coagulation disorders. On the other hand, pregnancy planning is an increasingly frequent concern. All patients should undergo genetic counseling, and it is important to monitor the appearance or worsening of organomegaly, bone and hematologic abnormalities to establish clinical and therapeutic recommendations. Management during the puerperium will depend on the evolution of gestation, and, during the lactation period, the potential appearance of bone complications should be assessed. An early onset of menopause, compared to the general population, has also been described, which may accelerate the development of osteopenia. Finally, although the usual screening protocols for neoplasms are currently being performed, it is recommended to watch for early signs of liver or renal neoplasms when examining the results of imaging tests performed during evaluations for this disease.

摘要

戈谢病是一种遗传性疾病,因缺乏葡糖脑苷脂酶导致葡糖神经酰胺蓄积。尽管目前已有大量科学证据,但关于该病对女性不同生命阶段的影响的数据仍然有限。除其他改变外,已有月经初潮延迟的描述,不过这与生育问题无关。月经过多相对常见,与血小板减少、血小板病或凝血障碍有关。另一方面,妊娠规划日益受到关注。所有患者均应接受遗传咨询,监测器官肿大、骨骼和血液学异常的出现或恶化情况对于制定临床和治疗建议很重要。产褥期的管理将取决于妊娠进展情况,哺乳期则应评估骨并发症的潜在出现情况。与普通人群相比,该病患者也有更早出现绝经的描述,这可能加速骨质减少的发展。最后,尽管目前正在执行常规的肿瘤筛查方案,但在检查该病评估期间进行的影像学检查结果时,建议留意肝脏或肾脏肿瘤的早期迹象。

相似文献

1
Women with Gaucher Disease.
Biomedicines. 2024 Mar 5;12(3):579. doi: 10.3390/biomedicines12030579.
2
The female Gaucher patient: the impact of enzyme replacement therapy around key reproductive events (menstruation, pregnancy and menopause).
Blood Cells Mol Dis. 2009 Nov-Dec;43(3):264-88. doi: 10.1016/j.bcmd.2009.04.003. Epub 2009 Jun 6.
4
[Gaucher disease: A review].
Rev Med Interne. 2019 May;40(5):313-322. doi: 10.1016/j.revmed.2018.11.012. Epub 2019 Jan 11.
5
Pulmonary Involvement Responsive to Enzyme Replacement Therapy in an Elderly Patient with Gaucher Disease.
Eur J Case Rep Intern Med. 2021 Sep 8;8(9):002802. doi: 10.12890/2021_002802. eCollection 2021.
7
Revised recommendations for the management of Gaucher disease in children.
Eur J Pediatr. 2013 Apr;172(4):447-58. doi: 10.1007/s00431-012-1771-z. Epub 2012 Jul 8.
8
Hematological manifestations and complications of Gaucher disease.
Expert Rev Hematol. 2016 Jan;9(1):51-8. doi: 10.1586/17474086.2016.1112732. Epub 2015 Nov 13.
9
A Review of Gaucher Disease Pathophysiology, Clinical Presentation and Treatments.
Int J Mol Sci. 2017 Feb 17;18(2):441. doi: 10.3390/ijms18020441.
10
Enzyme replacement and substrate reduction therapy for Gaucher disease.
Cochrane Database Syst Rev. 2015 Mar 27;2015(3):CD010324. doi: 10.1002/14651858.CD010324.pub2.

引用本文的文献

1
Age-related inflammatory biomarkers in early-onset osteoporosis in females with Gaucher disease.
Front Endocrinol (Lausanne). 2025 Jul 2;16:1606218. doi: 10.3389/fendo.2025.1606218. eCollection 2025.
2
Gaucher disease, state of the art and perspectives.
J Intern Med. 2025 Sep;298(3):155-172. doi: 10.1111/joim.20114. Epub 2025 Jul 3.
3
The multifaceted challenges faced by women in the field of inherited metabolic disorders.
Orphanet J Rare Dis. 2025 Mar 5;20(1):104. doi: 10.1186/s13023-025-03604-8.

本文引用的文献

1
Recommendations for oral treatment for adult patients with type 1 Gaucher disease.
Rev Clin Esp (Barc). 2022 Nov;222(9):529-542. doi: 10.1016/j.rceng.2022.02.008. Epub 2022 Jun 5.
2
Contraceptive use in women with inherited metabolic disorders: a retrospective study and literature review.
Orphanet J Rare Dis. 2022 Feb 8;17(1):41. doi: 10.1186/s13023-022-02188-x.
3
Hormone replacement therapy - Current recommendations.
Best Pract Res Clin Obstet Gynaecol. 2022 May;81:8-21. doi: 10.1016/j.bpobgyn.2021.12.001. Epub 2021 Dec 14.
4
Platelet Activation and Reactivity in a Large Cohort of Patients with Gaucher Disease.
Thromb Haemost. 2022 Jun;122(6):951-960. doi: 10.1055/a-1642-4206. Epub 2021 Nov 5.
5
Clinicogenetic Profile, Treatment Modalities, and Mortality Predictors of Gaucher Disease: A 15-Year Retrospective Study.
Public Health Genomics. 2021;24(3-4):139-148. doi: 10.1159/000514507. Epub 2021 Apr 6.
6
Pregnancy outcome in women with Gaucher disease type 1 who had unplanned pregnancies during eliglustat clinical trials.
JIMD Rep. 2020 Oct 18;57(1):76-84. doi: 10.1002/jmd2.12172. eCollection 2021 Jan.
7
Gaucher disease: Basic and translational science needs for more complete therapy and management.
Mol Genet Metab. 2021 Feb;132(2):59-75. doi: 10.1016/j.ymgme.2020.12.291. Epub 2020 Dec 29.
8
Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study.
J Genet Couns. 2021 Jun;30(3):755-765. doi: 10.1002/jgc4.1366. Epub 2020 Dec 15.
9
Unraveling the mystery of Gaucher bone density pathophysiology.
Mol Genet Metab. 2021 Feb;132(2):76-85. doi: 10.1016/j.ymgme.2020.07.011. Epub 2020 Aug 1.
10
Coagulation Parameters in Adult Patients With Type-1 Gaucher Disease.
J Hematol. 2019 Sep;8(3):121-124. doi: 10.14740/jh543. Epub 2019 Sep 30.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验