Lipedema and Klinefelter Syndrome in Two Morbidly Obese Patients
Resource type
Authors/contributors
- Cadart, Olivier (Author)
- Le Moal, Cyril (Author)
- Michelet, Marie (Author)
- Bosc, Laurène (Author)
- Pupier, Emilie (Author)
- Monsaingeon-Henry, Maud (Author)
- Gatta-Cherifi, Blandine (Author)
Title
Lipedema and Klinefelter Syndrome in Two Morbidly Obese Patients
Abstract
Introduction: Lipedema is an abnormal deposit of subcutaneous fat most often involving the lower limbs symmetrically. The physiopathology is poorly understood, but its peak of the almost exclusively female involvement and its peak of appearance at puberty, during pregnancy or at menopause orient toward a hormonal involvement, whereas other elements are in favor of a strong genetic predisposition. Klinefelter syndrome (KS) is a genetic disease linked to aneuploidy resulting in a karyotype 47 XXY most of the time. There is a substantial variation in clinical presentation, but it often features infertility, firm testicular hypotrophy, hypergonadotropic hypogonadism, gynecomastia, and learning difficulties. Many other pathologies are associated with KS, but lipedema is never mentioned and there are no data in the literature linking these two pathologies.
Publication
Androgens: Clinical Research and Therapeutics
Volume
2
Issue
1
Pages
134-140
Date
2021-08-01
Journal Abbr
Androgens: Clinical Research and Therapeutics
Language
en
ISSN
2689-4653
Accessed
9/2/21, 4:38 PM
Library Catalog
DOI.org (Crossref)
Citation
Cadart, O., Le Moal, C., Michelet, M., Bosc, L., Pupier, E., Monsaingeon-Henry, M., & Gatta-Cherifi, B. (2021). Lipedema and Klinefelter Syndrome in Two Morbidly Obese Patients. Androgens: Clinical Research and Therapeutics, 2(1), 134–140. https://doi.org/10.1089/andro.2021.0012
Topic
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