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Relevant bibliographies by topics / Acquired partial lipodystrophy

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Academic literature on the topic 'Acquired partial lipodystrophy'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Acquired partial lipodystrophy"

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Orrell, Richard W., Richard C. Peatfield, Carole E. Collins, et al. "Myopathy in acquired partial lipodystrophy." Clinical Neurology and Neurosurgery 97, no. 2 (1995): 181–86. http://dx.doi.org/10.1016/0303-8467(95)00021-b.

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Sorkina, Ekaterina L., and Anatoly N. Tiulpakov. "Inherited and acquired lipodystrophies: molecular-genetic and autoimmune mechanisms." Obesity and metabolism 15, no. 1 (2018): 39–42. http://dx.doi.org/10.14341/omet2018139-42.

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Lipodystrophy syndromes form a heterogenous group of inherited or acquired rare disorders, characterized by total (generalized lipodystrophy) or partial fat loss (partial lipodystrophy), usually accompanied by different metabolic disorders. Based on etiology lipodystrophies can be inherited or acquired. As a result of a significant progress in molecular genetics 20 new genes, associated with different lipodystrophy syndromes, were discovered during the last 20 years. However according to the majority of researchers data mutations in these causative genes are not found in approximately half of

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3

Muto, Yusuke, Taku Fujimura, Aya Kakizaki, Kenichiro Tsuchiyama, Yoshiyuki Kusakari, and Setsuya Aiba. "Adult-Onset Acquired Partial Lipodystrophy Accompanied by Rheumatoid Arthritis." Case Reports in Dermatology 7, no. 1 (2015): 70–74. http://dx.doi.org/10.1159/000381844.

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Lipodystrophy is a group of metabolic disorders, possibly caused by autoimmune disease. In this report, we describe a case of adult-onset acquired partial lipodystrophy accompanied by rheumatoid arthritis without a family history. Interestingly, immunohistochemical staining revealed dense infiltration of IL-27-producing cells as well as MMP-7- and MMP-28-expressing cells, both of which have been reported to facilitate the development of autoimmune disease. Our present case might suggest possible mechanisms for acquired partial lipodystrophy.

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YORULMAZ, Ahu, Esra ARI, and Başak YALÇIN. "Acquired Partial Lipodystrophy with Autoimmune Thyroiditis." Turkiye Klinikleri Journal of Case Reports 26, no. 3 (2018): 156–60. http://dx.doi.org/10.5336/caserep.2018-59805.

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Broadhead, Geoffrey K., and Andrew Chang. "Choroidal Neovascularization in Acquired Partial Lipodystrophy." European Journal of Ophthalmology 23, no. 3 (2013): 439–41. http://dx.doi.org/10.5301/ejo.5000271.

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Patel, D., and B. Page. "Ocular complications in acquired partial lipodystrophy." Postgraduate Medical Journal 82, no. 973 (2006): 774. http://dx.doi.org/10.1136/pgmj.2006.047001.

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Dizdarer, Ceyhun, Sema Kalkan, Tugrul Ozcan, Demet Tumay, and Safiye Aktas. "Acquired Partial Lipodystrophy Associated With Hypocomplementemia." Laboratory Medicine 36, no. 9 (2005): 546–49. http://dx.doi.org/10.1309/0yu3xdv37gab08kh.

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8

Karunaratne, Yasiru Gehan, Marc Langbart, Jerry R. Greenfield, and James Southwell-Keely. "Large-volume liposuction in acquired partial lipodystrophy." Australasian Journal of Plastic Surgery 2, no. 2 (2019): 67–69. http://dx.doi.org/10.34239/ajops.v2n2.14.

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9

Alraddadi, Raghad Awad. "Overview on Acquired Partial Lipodystrophy: Review Article." Egyptian Journal of Hospital Medicine 91, no. 1 (2023): 4242–45. http://dx.doi.org/10.21608/ejhm.2023.296194.

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10

Garg, Abhimanyu. "Lipodystrophies: Genetic and Acquired Body Fat Disorders." Journal of Clinical Endocrinology & Metabolism 96, no. 11 (2011): 3313–25. http://dx.doi.org/10.1210/jc.2011-1159.

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Abstract Context: Lipodystrophies are heterogeneous, genetic or acquired disorders characterized by selective loss of body fat and predisposition to insulin resistance. The extent of fat loss determines the severity of associated metabolic complications such as diabetes mellitus, hypertriglyceridemia, and hepatic steatosis. Evidence Acquisition and Synthesis: Both original and review articles were found via PubMed search reporting on clinical features and management of various types of lipodystrophies and were integrated with the author's knowledge of the field. Conclusion: The autosomal reces

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Book chapters on the topic "Acquired partial lipodystrophy"

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"Acquired partial lipodystrophy." In Dermatology Therapy. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/3-540-29668-9_41.

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Mattingly, Megan, Areli Valencia, Elaine Cochran, Rebecca J. Brown, and Phillip Gorden. "The Lipodystrophy Syndromes: Clinical Features and Treatments." In Atypical Diabetes: Pathophysiology, Clinical Presentations, and Treatment Options. American Diabetes Association, 2018. http://dx.doi.org/10.2337/9781580406666.ch03.

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The lipodystrophies are a heterogeneous group of conditions characterized by loss of adipose tissue and, usually, metabolic disturbance. They are subdivided into generalized and partial forms with further subdivision into congenital (gene mutations) or acquired (autoimmune) forms.(1-11) Considerable progress has been made in describing new genetic abnormalities in both the generalized (GLD) and partial lipodystrophies (PLD ). Historically, the genetic forms of GLD have been referred to as the Berardinelli-Seip syndrome, but are more appropriately characterized by their genetic etiology.

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3

Swe, NM, KC Chiu, M. Htut, and E. Ipp. "Severe Insulin Resistance and Hypertriglyceridemia with Acquired Partial Lipodystrophy after Allogenic Bone Marrow Transplant." In The Endocrine Society's 92nd Annual Meeting, June 19–22, 2010 - San Diego. Endocrine Society, 2010. http://dx.doi.org/10.1210/endo-meetings.2010.part3.p12.p3-565.

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Conference papers on the topic "Acquired partial lipodystrophy"

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Bakewell, Christopher, Astor Rodrigues, Rachel Williams, Girish Gupte, Kavinda Dayasiri, and Geetha Anand. "P03 A curious case of autoimmune hepatitis and acquired partial lipodystrophy." In Abstracts of the BSPGHAN Virtual Annual Meeting, 27–29 April 2021. BMJ Publishing Group Ltd, 2021. http://dx.doi.org/10.1136/flgastro-2021-bspghan.14.

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