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Results 1 - 10 of 20 for lipoatrophy
  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 
    ... a lack of fatty tissue under the skin (lipoatrophy), primarily in the face, arms, and chest. This ... and problems with adipocyte maturation might contribute to lipoatrophy in affected individuals. It is unclear how reduced ...
    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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