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lipodystrofia familiárna čiastočná

  1. Subject h.lipodystrofia familiárna čiastočná
    Subject h.Lipodystrophy, Familial Partial
    Entry termslipodystrofia familiárna parciálna
    Scope note in EnglishInherited conditions characterized by the partial loss of ADIPOSE TISSUE, either confined to the extremities with normal or increased fat deposits on the face, neck and trunk (type 1), or confined to the loss of SUBCUTANEOUS FAT from the limbs and trunk (type 2). Type 3 is associated with mutation in the gene encoding PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA.
    See also reference (FX) in Slovak PPAR gama
    See also reference (FX) in English PPAR gamma
    Links (1) - MeSH descriptor
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Number of the records: 1  

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