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pmid: 34728268
Lipodystrophy syndromes are rare complex multisystem disorders caused by generalized or partial lack of adipose tissue. Adipose tissue dysfunction in lipodystrophy is associated with leptin deficiency. Lipodystrophy leads to severe metabolic problems. These abnormalities include, but are not limited to, insulin-resistant diabetes, severe hypertriglyceridemia, and lipid accumulation in ectopic organs such as the liver, and are associated with end-organ complications. Metabolic abnormalities can be present at the time of diagnosis or may develop over time as the disease progresses. In addition to metabolic abnormalities, subtype-specific presentations due to underlying molecular etiology in genetic forms and autoimmunity in acquired forms contribute to severe morbidity in lipodystrophy.
Hypertriglyceridemia, Leptin, Metabolic Syndrome, Heart Diseases, Lipodystrophy, Neuromuscular Diseases, Syndrome, Lipid Metabolism, Autoimmune Diseases, Liver, Pancreatitis, Non-alcoholic Fatty Liver Disease, Diabetes Mellitus, Humans, Kidney Diseases, Insulin Resistance
Hypertriglyceridemia, Leptin, Metabolic Syndrome, Heart Diseases, Lipodystrophy, Neuromuscular Diseases, Syndrome, Lipid Metabolism, Autoimmune Diseases, Liver, Pancreatitis, Non-alcoholic Fatty Liver Disease, Diabetes Mellitus, Humans, Kidney Diseases, Insulin Resistance
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 8 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |