CareLit · DOI-Nachweis · Diabetologie und Stoffwechsel
Metabolic phenotypes in male subjects with Dunnigan type of familial partial Lipodystrophy due to a lamin A/C R482W mutation
DOI 10.1055/s-0029-1221801
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Autor:innenDM Schulte, F Oberhäuser, K Walgenbach, M Faust, M Schubert, W Krone, M Laudes
ZeitschriftDiabetologie und Stoffwechsel
Ausgabe05/2009
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Context: Familial partial lipodystrophy (FPLD) is a genetically determined disease with defects in body fat distribution and metabolic abnormalities caused by mutations in lamin A/C. Although lamin A/C R482W is autosomal inherited, in a previous report male subjects were reported not to be metabolically affected suggesting male carriers do not need specialized endocrine care. The aim of the present study was to char…
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Zitierempfehlung
DM Schulte, F Oberhäuser, K Walgenbach, M Faust, M Schubert, W Krone, M Laudes (2009) Metabolic phenotypes in male subjects with Dunnigan type of familial partial Lipodystrophy due to a lamin A/C R482W mutation. Diabetologie und Stoffwechsel (05). https://doi.org/10.1055/s-0029-1221801
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