Other Names for this Disease
- Lipodystophy partial progressive
- Lipodystrophy cephalothoracic type
- Lipodystrophy partial acquired
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lipodystrophy, is characterized by the loss of fat from the face, neck, shoulders, arms, forearms, chest and abdomen. Occasionally the groin or thighs are also affected. Onset usually begins in childhood following a viral illness. It affects females more often than males. The fat loss usually has a 18 month course, but can come and go over the course of several years. Following puberty, affected women may experience a disproportionate accumulation of fat in the hips and lower limbs. Around 1 in 5 people with this syndrome develop membranoproliferative glomerulonephritis. This kidney condition usually develops more than 10 years after the lipodystrophy's onset. Autoimmune disorders may also occur in association with this syndrome.Barraquer-Simons syndrome, or acquired partial
Last updated: 7/29/2011
- Acquired: Partial Lipodystrophy (Barraquer-Simons Syndrome). The University of Texas Southwestern Medical Center at Dallas Web site. 2007; http://www.utsouthwestern.edu/media/files/2400/Partial-Lipo-Barraquer-Simons-Syndrome.pdf. Accessed 7/29/2011.
- DermNet NZ is an online resource about skin diseases developed by the New Zealand Dermatological Society Incorporated. DermNet NZ provides information about this condition.
- Genetics Home Reference (GHR) contains information on Barraquer-Simons syndrome. This website is maintained by the National Library of Medicine.
- The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
- Medscape Reference provides information on this topic. You may need to register to view the medical textbook, but registration is free.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Barraquer-Simons syndrome. Click on the link to view a sample search on this topic.
- The University of Texas Southwestern Medical Center Web site provides a diagram of how Barraquer-Simons syndrome may affect the body. Click on the link above to view the illustration.