A retrospective cohort study evaluating pregnancy outcomes in women with MIDD
Author:
Funder
Health Research Board
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00592-023-02202-z.pdf
Reference38 articles.
1. Ng YS, Lim AZ, Panagiotou G et al (2022) Endocrine manifestations and new developments in mitochondrial disease. Endocr Rev. https://doi.org/10.1210/endrev/bnab036
2. Murphy R, Turnbull DM, Walker M, Hattersley AT (2008) Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation. Diabet Med. https://doi.org/10.1111/j.1464-5491.2008.02359.x
3. Mezghani N, Mnif M, Mkaouar-Rebai E et al (2013) A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions. Biochem Biophys Res Commun. https://doi.org/10.1016/j.bbrc.2013.01.063
4. Li Yee M, Wong R, Datta M et al (2018) Mitochondrial disease: an uncommon but important cause of diabetes mellitus. Endocrinol Diabetes Metab Case Rep. https://doi.org/10.1530/EDM-18-0091
5. Nesbitt V, Pitceathly RDS, Turnbull DM et al (2013) The UK MRC mitochondrial disease patient cohort study: clinical phenotypes associated with the m.3243A>G mutation - implications for diagnosis and management. J Neurol Neurosurg Psychiatry. https://doi.org/10.1136/jnnp-2012-303528
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Obstetric complications in women with mitochondrial disease;Acta Diabetologica;2024-01-18
2. MIDD due to variants m.3243A > G or m.12258C > A not necessarily carries an increased risk of obstetric complications;Acta Diabetologica;2023-12-14
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