Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 4 of 4 for "Lipodystrophy," familial "partial," type 8
  1. LMNA gene 
    ... the LMNA gene have been found to cause familial partial lipodystrophy type 2 (also known as familial partial lipodystrophy, Dunnigan type), a rare condition characterized by an abnormal distribution ...
    https://medlineplus.gov/genetics/gene/lmna - Genetics
  2. CAV1 gene 
    ... VIP21 Tests of CAV1 PubMed CAVEOLIN 1; CAV1 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 7; FPLD7 NCBI Gene ClinVar Boscher C, Nabi IR. Caveolin-1: role in cell signaling. Adv Exp Med Biol. 2012;729:29-50. doi: ... partial lipodystrophy and hypertriglyceridemia. Lipids Health Dis. 2008 Jan 31; ...
    https://medlineplus.gov/genetics/gene/cav1 - Genetics
  3. Nakajo-Nishimura syndrome 
    ... assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation ... and progressive partial lipodystrophy. Allergol Int. 2012 Jun;61(2):197-206. ...
    https://medlineplus.gov/genetics/condition/nakajo-nishimura-syndrome - Genetics
  4. C3 glomerulopathy 
    ... people with dense deposit disease may have acquired partial lipodystrophy, a condition characterized by a lack of fatty ( ... can occur with dense deposit disease, including acquired partial lipodystrophy and a buildup of drusen in the retina. ...
    https://medlineplus.gov/genetics/condition/c3-glomerulopathy - Genetics