A promising treatment for spontaneous ovarian hyperstimulation syndrome due to familial partial lipodystrophy: GnRH analogs combined with cyst aspiration
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s42000-023-00469-z.pdf
Reference17 articles.
1. Brown RJ, Araujo-Vilar D, Cheung PT, Dunger D, Garg A, Jack M et al (2016) The diagnosis and management of lipodystrophy syndromes: a Multi-Society Practice Guideline. J Clin Endocrinol Metab 101(12):4500–4511. https://doi.org/10.1210/jc.2016-2466
2. Dunnigan MG, Cochrane MA, Kelly A, Scott JW (1974) Familial lipoatrophic diabetes with dominant transmission. New Syndr Q J Med 43(169):33–48
3. Garg A, Peshock RM, Fleckenstein JL (1999) Adipose tissue distribution pattern in patients with familial partial lipodystrophy (Dunnigan variety). J Clin Endocrinol Metab 84(1):170–174. https://doi.org/10.1210/jcem.84.1.5383
4. Boschmann M, Engeli S, Moro C, Luedtke A, Adams F, Gorzelniak K et al (2010) LMNA mutations, skeletal muscle lipid metabolism, and insulin resistance. J Clin Endocrinol Metab 95(4):1634–1643. https://doi.org/10.1210/jc.2009-1293
5. Garg A, Vinaitheerthan M, Weatherall PT, Bowcock AM (2001) Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene. J Clin Endocrinol Metab 86(1):59–65. https://doi.org/10.1210/jcem.86.1.7121
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