Lipedema: an inherited condition.

Resource type
Authors/contributors
Title
Lipedema: an inherited condition.
Abstract
Lipedema is a condition characterized by swelling and enlargement of the lower limbs due to abnormal deposition of subcutaneous fat. Lipedema is an under-recognized condition, often misdiagnosed as lymphedema or dismissed as simple obesity. We present a series of pedigrees and propose that lipedema is a genetic condition with either X-linked dominant inheritance or more likely, autosomal dominant inheritance with sex limitation. Lipedema appears to be a condition almost exclusively affecting females, presumably estrogen-requiring as it usually manifests at puberty. Lipedema is an entity distinct from obesity, but may be wrongly diagnosed as primary obesity, due to clinical overlap. The phenotype suggests a condition distinct from obesity and associated with pain, tenderness, and easy bruising in affected areas.
Publication
American journal of medical genetics. Part A
Volume
152A
Issue
4
Pages
970-976
Date
2010 Apr
Journal Abbr
Am J Med Genet A
Language
eng
ISSN
1552-4833 1552-4825
Archive
lipoedem-hilfe-ev
Rights
(c) 2010 Wiley-Liss, Inc.
Extra
Place: United States
Citation
Child, A. H., Gordon, K. D., Sharpe, P., Brice, G., Ostergaard, P., Jeffery, S., & Mortimer, P. S. (2010). Lipedema: an inherited condition. American Journal of Medical Genetics. Part A, 152A(4), 970–976. lipoedem-hilfe-ev. https://doi.org/10.1002/ajmg.a.33313