Diagnosis and management of lipodystrophy: a practical update
Author:
Affiliation:
1. Wolfson Department of Diabetes & Endocrinology, Box 289, Level 4, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke’s Hospital, Cambridge CB2 0QQ, UK
Publisher
Informa UK Limited
Subject
Cardiology and Cardiovascular Medicine,Endocrinology, Diabetes and Metabolism
Link
https://www.tandfonline.com/doi/pdf/10.2217/clp.14.13
Reference131 articles.
1. Garg A. Clinical review: lipodystrophies: genetic and acquired body fat disorders. J. Clin. Endocrinol. Metab. 96(11), 3313–3325 (2011). • A review of the classification, clinical features and molecular basis of lipodystrophies.
2. Nolis T. Exploring the pathophysiology behind the more common genetic and acquired lipodystrophies. J. Hum. Genet. 59(1), 16–23 (2013). • Useful review including a description of normal adipocyte differentiation and regulation, and the underlying mechanisms responsible for the pathophysiology of lipodystrophy syndromes.
3. Strickland LR, Guo F, Lok K, Garvey WT. Type 2 diabetes with partial lipodystrophy of the limbs: a new lipodystrophy phenotype. Diabetes Care 36(8), 2247–2253 (2013).
4. Herbst KL, Tannock LR, Deeb SS, Purnell JQ, Brunzell JD, Chait A. Kobberling type of familial partial lipodystrophy: an underrecognized syndrome. Diabetes Care 26(6), 1819–1824 (2003).
5. Knebel B, Kotzka J, Lehr S et al. A mutation in the c-fos gene associated with congenital generalized lipodystrophy. Orphanet. J. Rare Dis. 8, 119 (2013).
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