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Results 1 - 10 of 10 for Lipodystrophy
  1. BSCL2 gene 
    ... have been identified in people with congenital generalized lipodystrophy (also called Berardinelli-Seip congenital lipodystrophy) type 2. This rare condition is characterized by ...
    https://medlineplus.gov/genetics/gene/bscl2 - Genetics
  2. CAV1 gene 
    ... gene has been found to cause congenital generalized lipodystrophy (also called Berardinelli-Seip congenital lipodystrophy) type 3. This rare condition is characterized by ...
    https://medlineplus.gov/genetics/gene/cav1 - Genetics
  3. AGPAT2 gene 
    ... have been identified in people with congenital generalized lipodystrophy (also called Berardinelli-Seip congenital lipodystrophy) type 1. This rare condition is characterized by ...
    https://medlineplus.gov/genetics/gene/agpat2 - Genetics
  4. CAVIN1 gene 
    ... gene have been found to cause congenital generalized lipodystrophy (also called Berardinelli-Seip congenital lipodystrophy) type 4. This rare condition is characterized by ...
    https://medlineplus.gov/genetics/gene/cavin1 - Genetics
  5. PSMB8 gene 
    ... and wasting and a loss of fatty tissue (lipodystrophy), mainly in the upper body. Because the protein ... contractures, muscular atrophy, microcytic anemia, and panniculitis-induced lipodystrophy (JMP) syndrome; and the other called chronic atypical ...
    https://medlineplus.gov/genetics/gene/psmb8 -
  6. LMNA gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/lmna - Genetics
  7. ZMPSTE24 gene 
    ... mandibuloacral dysplasia called mandibuloacral dysplasia with type B lipodystrophy (MADB). This condition is characterized by a variety ... affecting all parts of the body (type B lipodystrophy). ZMPSTE24 gene mutations that cause MADB lead to ...
    https://medlineplus.gov/genetics/gene/zmpste24 - Genetics
  8. PIK3R1 gene 
    ... Molven A, Njolstad PR. SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. Am ...
    https://medlineplus.gov/genetics/gene/pik3r1 - Genetics
  9. SLC25A24 gene 
    ... a lack of fatty tissue under the skin (lipodystrophy), excessive hair growth (hypertrichosis) on the face and ...
    https://medlineplus.gov/genetics/gene/slc25a24 - Genetics
  10. POLR3A gene 
    ... a lack of fatty tissue under the skin (lipodystrophy), sparse hair on their head, and abnormal tooth ...
    https://medlineplus.gov/genetics/gene/polr3a - Genetics