- A Case of Centrifugal Lipodystrophy with Apoptotic Process in the Fatty Tissue
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Cho HS, Park EJ, Kim CW, Kim KH, Kim KJ
- KMID: 2158455
- Ann Dermatol.
- 2005 Dec;17(2):92-94.
- doi: 10.5021/ad.2005.17.2.92
No abstract available. -
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- Idiopathic Localized Lipodystrophy of Subcutaneous Fat after Cyst Enucleation of Jaw: Report of 3 Cases
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Lee B, Na HY, Kim NK, Kim HJ
- KMID: 1969976
- J Korean Assoc Maxillofac Plast Reconstr Surg.
- 2012 May;34(3):205-208.
Lipodystrophy is a disorder characterized by the loss of subcutaneous adipose tissue which is inherited or heterogeneously acquired. We report 3 uncommon cases of localized lipodystrophy on face which distinguished... -
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- Four Cases of Steroid-Induced Lipodystrophy
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Kim YH, Kim GM, Choi YY, Hwang TJ
- KMID: 1661925
- J Korean Pediatr Soc.
- 1995 Jun;38(6):843-847.
No abstract available. -
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- A Case of Familial Partial Lipodystrophy
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Kim DH, Ahn WK, Kim CW, Kim TY
- KMID: 2086283
- Korean J Dermatol.
- 1999 Dec;37(12):1841-1843.
Partial lipodystrophy(PLD) is a rare disorder characterized by frequent occurrence in women, usually onset in childhood, and slowly progressive symmetrical loss of subcutaneous fat on the upper half of the... -
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- A case of generalized lipodystrophy
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Chang SH, Youn JI, Lee YS
- KMID: 1692701
- Korean J Dermatol.
- 1991 Apr;29(2):241-246.
Generalized lipodyst,rophy is characterized by generalized loss of body fat, and is asociated vith metabolic ahnormalities, including insulin resistance, hyperglycemia., and hypertriglyceridemia. like acanthosis nigricans, generalized lipodystrophy is a cutaneous... -
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- A Case of Membranous Lipodystrophy with Sporotrichosis
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Shin NL, Choi YW, Choi HY, Myung KB
- KMID: 2303223
- Korean J Dermatol.
- 2000 Aug;38(8):1111-1112.
No abstract available. -
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- Acquired Partial Lipodystrophy (Barraquer-Simons Syndrome): Early Cosmetic Intervention with Autologous Fat
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Rho NK, Kim WS
- KMID: 2419755
- Ann Dermatol.
- 2018 Oct;30(5):610-613.
- doi: 10.5021/ad.2018.30.5.610
Barraquer-Simons syndrome is a rare acquired lipodystrophy characterized by gradually symmetric subcutaneous fat loss in a craniocaudal distribution, often associated with hypocomplementemia and nephropathies. Facial cosmetic treatment in this disorder... -
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- Three Cases of Secondary Membranous Lipodystrophy
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Seo SL, Kim MH, Lim YS, Choi HY, Myung KB
- KMID: 1548206
- Korean J Dermatol.
- 1999 Jan;37(1):91-96.
Membranous lipodystrophy is a peculiar type of fat necrosis, present in patients with various types of skin diseases. It is charaeterized by the presence of microcysts and macrocysts lined by... -
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- Acquired Generalized Lipodystrophy with Severe Insulin Resistant Diabetes Mellitus
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Lee JM, Sohn TS, Son HS
- KMID: 2331798
- J Korean Diabetes Assoc.
- 2006 Nov;30(6):487-491.
Acquired generalized lipodystrophy is a rare disease, and often follows autoimmune disease, prodromal infection, HIV infection. The clinical characteristics are generalized absence of fat, insulin resistance, diabetes mellitus, absence of... -
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- A Case of Congenital Generalized Lipodystrophy
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Kim WS, Kim KT, Ahn DH, Sohn KC
- KMID: 2103986
- J Korean Pediatr Soc.
- 1981 Feb;24(2):173-180.
No abstract available. -
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- A Case of Berardinelli Lipodystrophy Syndrome
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Hwang JS, Lim JS, Kim SY, Shim KS, Yang SW, Yu JS
- KMID: 1529898
- J Korean Soc Pediatr Endocrinol.
- 1997 Sep;2(2):274-276.
Berardinelli lipodystrophy syndrome is a rare autosomal recessive disorder, characterized by loss of body fat, muscular hypertrophy, acanthosis nigricans, hepatomegaly, hyperlipidemia, insulin resistant diabetes, and elevated metabolic rate. The mechanism(s)... -
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- A Case of Membranous Lipodystrophy with Stasis Dermatitis
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Lee JW, Choi EH, Ahn SK
- KMID: 2086719
- Korean J Dermatol.
- 2003 Sep;41(9):1220-1223.
Membranous lipodystrophy is a peculiar type of fat necrosis, present in patients with various types of skin disease. It is characterized by the presence of microcysts and macrocysts lined by... -
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- A Case of Membranous Lipodystrophy Observed in Lichen Amyloidosis
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Lee Y, Ahn SY, Ji JH, Hong SP, Bak H, Lee SH, Ahn SK
- KMID: 2219390
- Ann Dermatol.
- 2009 May;21(2):174-177.
- doi: 10.5021/ad.2009.21.2.174
Membranous lipodystrophy is characterized by the presence of microcysts lined by amorphous, eosinophilic material with an arabesque appearance. We experienced a case of a 72-year-old man who had dark brownish,... -
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- A Case of progressive Lipodystrophy
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Cho BK, Houh W
- KMID: 1664296
- Korean J Dermatol.
- 1973 Oct;11(2):101-104.
A case of progressive lipodystrophy affecting 19-year-old female, is reported. Two years ago, she accidentally discovered brownish pigmented, and depressed lesion on the periumbilical area. For one year after that,... -
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- A Case of Partial Lipodystrophy
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Mok HS, Kwon KS, Chung TA
- KMID: 1679456
- Korean J Dermatol.
- 1985 Dec;23(6):817-821.
Partial lipodystrophy is an uncommon disorder primarily affecting women, with onset usually in childhood, characterized by slowly progressive, symrnetrical loss of aubcutaneous fat from the upper half of the body.... -
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- Leptin in Relation to the Lipodystrophy-Associated Metabolic Syndrome
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Mantzoros
- KMID: 2281398
- Diabetes Metab J.
- 2012 Jun;36(3):181-189.
- doi: 10.4093/dmj.2012.36.3.181
Leptin, an adipocyte-secreted hormone, regulates energy homeostasis as well as reproductive, neuroendocrine, immune and metabolic functions. Subjects with decreased amounts of fat in their adipose tissue, i.e., lipoatrophy, have low... -
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- An Unusual Case with Membranous Lipodystrophy in a Hypertensive Patient with Transepidermal Elimination
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Bak H, Lee JW, Ahn HJ, Hwang SM, Choi EH, Lee SH, Ahn SK
- KMID: 1715864
- Yonsei Med J.
- 2006 Jun;47(3):428-431.
- doi: 10.3349/ymj.2006.47.3.428
Membranous lipodystrophy represents a peculiar type of fat necrosis that is present in patients with various types of skin disease. It is characterized by the presence of microcysts and macrocysts... -
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- A case of lipodystrophy centrifugalis abdominalis infantilis
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Suh MK, Kim NH
- KMID: 1692702
- Korean J Dermatol.
- 1991 Apr;29(2):247-251.
We report a case of lipodystrophia centrifugalis abdomina]is infantilis in a 2 year 5 month male. At age 7 months, his parents noticed a bluish macule in the right inguinal... -
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- Novel LMNA Gene Mutation in a Patient With Atypical Werner's Syndrome
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Doh YJ, Kim HK, Jung ED, Choi SH, Kim JG, Kim BW, Lee IK
- KMID: 1785645
- Korean J Intern Med.
- 2009 Mar;24(1):68-72.
- doi: 10.3904/kjim.2009.24.1.68
Hutchinson-Gilford progeria syndrome (HGPS) and Werner's syndrome are representative types of progeroid syndrome. LMNA (Lamin A/C) gene mutation with atypical Werner's syndrome have recently been reported. Atypical Werner's syndrome with... -
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- Concurrent SHORT syndrome and 3q duplication syndrome
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Boaz AM, Grasso SA, DeRogatis , Beesley EN
- KMID: 2451621
- J Genet Med.
- 2019 Jun;16(1):15-18.
- doi: 10.5734/JGM.2019.16.1.15
SHORT syndrome is an extremely rare congenital condition due to a chromosomal mutation of the PIK3R1 gene found at 5q13.1. SHORT is a mnemonic representing six manifestations of the syndrome:... -
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