A cohort analysis of familial partial lipodystrophy from two Mediterranean countries

Aim To assess the disease burden of familial partial lipodystrophy (FPLD) caused by LMNA (FPLD2) and PPARG (FPLD3) variants to augment the knowledge of these rare disorders characterized by selective fat loss and metabolic complications. Materials and Methods An observational longitudinal study, inc...

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Veröffentlicht in:	Diabetes, obesity & metabolism obesity & metabolism, 2024-11, Vol.26 (11), p.4875-4886
Hauptverfasser:	Fernández‐Pombo, Antía, Yildirim Simsir, Ilgin, Sánchez‐Iglesias, Sofía, Ozen, Samim, Castro, Ana I., Atik, Tahir, Loidi, Lourdes, Onay, Huseyin, Prado‐Moraña, Teresa, Adiyaman, Cem, Díaz‐López, Everardo Josué, Altay, Canan, Ginzo‐Villamayor, Maria José, Akinci, Baris, Araújo‐Vilar, David
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Age Body mass index Cardiovascular disease Cohort Studies Coronary artery disease Coronary vessels Diabetes mellitus Diagnosis familial partial lipodystrophy Fatty liver Female Genotypes Heart diseases Humans hypertriglyceridaemia Hypertriglyceridemia - complications Hypertriglyceridemia - epidemiology Lamin Type A - genetics Lipodystrophy Lipodystrophy, Familial Partial - complications Lipodystrophy, Familial Partial - epidemiology Lipodystrophy, Familial Partial - genetics Liver diseases LMNA Longitudinal Studies Male metabolic abnormalities Metabolism Middle Aged Myocardial infarction Phenotypes PPARG Retinopathy Spain - epidemiology Steatosis Turkey - epidemiology Vein & artery diseases
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