Journals / Fiziksel Tıp ve Rehabilitasyon Bilimleri Dergisi / 2019 / Cilt: 22 - Sayı: 1

Barraquer-Simons Syndrome Occurred After Pregnancy: A Rare Case Report

Gebelik Sonrası Meydana Gelen Barraquer-Simons Sendromu: Nadir Görülen Bir Olgu

Pages
33–35
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this paper a 34-year-oldwoman with progresive loss of subcutaneous fat limited to upper arm, which was developed afterpregnancy, is reported and literature was reviewed.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Lipodystrophies are a widespread group of genetic or acquired metabolic disorders thatare characterized by varying degrees of body fat loss.
📊
Key Findings & Data:The Barraquer-Simons syndrome also calledAcquired Partial Lipodistrophy is a form of partial lipodistrophy of unknown etiology, characterisedby the loss of subcutaneous adipose tissue, limited to upper part of the body.
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Conclusion & Impact:In this paper a 34-year-oldwoman with progresive loss of subcutaneous fat limited to upper arm, which was developed afterpregnancy, is reported and literature was reviewed.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Lipodystrophies are a widespread group of genetic or acquired metabolic disorders thatare characterized by varying degrees of body fat loss. The Barraquer-Simons syndrome also calledAcquired Partial Lipodistrophy is a form of partial lipodistrophy of unknown etiology, characterisedby the loss of subcutaneous adipose tissue, limited to upper part of the body. Also it can be associatedwith hypocomplementemia, diabetes, and hypertriglyceridemia. In this paper a 34-year-oldwoman with progresive loss of subcutaneous fat limited to upper arm, which was developed afterpregnancy, is reported and literature was reviewed.

Özet

Lipodistrofiler genetik veya sonradan edinilen vücutta değişik derecelerde yağ doku kaybı ile seyreden bir grup metabolik bozukluklardır. Barraquer-Simons sendromu diğer ismi ile “Edinilmiş Parsiyel Lökodistrofi” parsiyel lökodistrofilerin bir formudur. Etiyolojisi bilinmemektedir ve genellikle üst ekstremitede yağ doku kaybı ile seyretmektedir. Bunun dışında hipokomplemantemi, diyabet ve hipertrigliseridemi ile ilişkili olabilmektedir. Bu yazıda gebelik sonrasında üst kolda ilerleyici subkutan yağ doku kaybı olan Barraquer-Simons sendromlu 34 yaşındaki kadın olgu sunulmuştur ve bu olgu ile ilgili literatür bilgileri gözden geçirilmiştir.

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Cite This Article

BATUR, E. B. (2022). Barraquer-Simons Syndrome Occurred After Pregnancy: A Rare Case Report. Fiziksel Tıp ve Rehabilitasyon Bilimleri Dergisi, Cilt: 22 - Sayı: 1, 33–35. https://ajindex.com/articles/508392

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References (16)

  1. Capeau J, Magré J, Caron-Debarle M, et al. Human lipodystrophies: genetic and acquired diseases of adipose tissue. Endocr Dev. 2010
  2. [Crossref] [PubMed] Garg A. Lipodystrophies: genetic and acquired body fat disorders. J Clin Endocrinol Metab. 2011
  3. [Crossref] [PubMed] Garg A. Lipodystrophies. Am J Med. 2000
  4. [Crossref] Oliveira J, Freitas P, Lau E, et al. Barraquer-Simons syndrome: a rare formof acquired lipodystrophy. BMC Res Notes. 2016
  5. Ferrarini A, Milani D, Bottigelli M, et al. Two new cases of Barraquer-Simons syndrome. Am J Med Genet. 2004
  6. 126A:427-9. [Crossref] [PubMed] Fardet L, Vigouroux C, Capeau J. Syndromes lipodystrophiques-Lipodystrophies. La Revue de Médecine Interne. 2013
  7. [Crossref] [PubMed] Requena Caballero C, Angel Navarro Mira M, Bosch IF, et al. Barraquer-Simons lipodystrophy associated with antiphospholipid syndrome. J Am Acad Dermatol. 2003
  8. [Crossref] Freitas P, Carvalho D. Lipodystrophy: beyond generalization? Panminerva Med. 2013
  9. [PubMed] Kim CA, Delepine M, Boutet E, et al. Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy. J Clin Endocrinol Metab. 2008
  10. [Crossref] [PubMed] Hayashi YK, Matsuda C, Ogawa M, et al. Human PTRF mutations cause secondary deficiency of caveolin resulting in muscular dystrophy with generalized lipodystrophy. J Clin Invest. 2009
  11. [Crossref] [PubMed] Subramanyam L, Simha V, Garg A. Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations. Clin Genet. 2010
  12. [Crossref] [PubMed] [PMC] Hegele RA, Cao H, Liu DM, et al. Sequencing of the reannotated LMNB2 gene reveals novel mutations in patients with acquired partial lipodystrophy. Am J Human Genet. 2006
  13. [Crossref] [PubMed] [PMC] Misra A, Peethambaram A, Garg A. Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature. Medicine (Baltimore). 2004
  14. [Crossref] [PubMed] Nolis T. Exploring the pathophysiology behind the more common genetic and acquired lipodystrophies. J Hum Genet. 2013
  15. [Crossref] [PubMed] Mathieson PW, Wurzner R, Oliveria DB, et al. Complement mediated adipocyte lysis by nephritic factor sera. J Exp Med. 1993
  16. [Crossref] [PubMed] Corvillo F, Aparicio V, Garrido S,