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Results 1 - 10 of 19 for Lipodystrophy
  1. Familial partial lipodystrophy 
    Familial partial lipodystrophy is a rare condition characterized by an abnormal distribution of fatty (adipose) tissue. Adipose tissue is normally found in many ...
    https://medlineplus.gov/.../condition/familial-partial-lipodystrophy - Genetics
  2. Congenital generalized lipodystrophy 
    Congenital generalized lipodystrophy (also called Berardinelli-Seip congenital lipodystrophy) is a rare condition characterized by an almost total lack of fatty ( ...
    https://medlineplus.gov/.../congenital-generalized-lipodystrophy - Genetics
  3. Nakajo-Nishimura syndrome 
    ... muscles, along with a loss of fatty tissue (lipodystrophy), mainly in the upper body. The combination of ... contractures, muscular atrophy, microcytic anemia, and panniculitis-induced lipodystrophy (JMP) syndrome; and the other called chronic atypical ...
    https://medlineplus.gov/genetics/condition/nakajo-nishimura-syndrome - Genetics
  4. 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
  5. Short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay 
    ... from one affected parent. Growth retardation-Rieger anomaly Lipodystrophy, partial, with Rieger anomaly and short stature Short ... Molven A, Njolstad PR. SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. Am ...
    https://medlineplus.gov/...ression-rieger-anomaly-and-teething-delay - Genetics
  6. 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
  7. 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
  8. Mandibuloacral dysplasia 
    ... a lack of fatty tissue under the skin (lipodystrophy) in certain regions of the body. The two ... of this disorder, mandibuloacral dysplasia with type A lipodystrophy (MADA) and mandibuloacral dysplasia with type B lipodystrophy ( ...
    https://medlineplus.gov/genetics/condition/mandibuloacral-dysplasia - Genetics
  9. 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
  10. 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 -
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