Phenotypic heterogeneity in patients with familial partial lipodystrophy (Dunnigan variety) related to the site of missense mutations in lamin A/C gene

Medicine & Life Sciences

• Familial Partial Lipodystrophy 100%
• Lamin Type A 80%
• Missense Mutation 59%
• Genes 23%
• Exons 18%
• lamin C 12%
• Fats 10%
• Body Fat Distribution 9%
• Buttocks 8%
• Anthropometry 8%
• Mutation 8%
• Siblings 6%
• HDL Cholesterol 6%
• Chromatin 6%
• Thigh 5%
• Triglycerides 5%
• Neck 5%
• Extremities 5%
• Proteins 5%
• Magnetic Resonance Imaging 4%
• Phenotype 4%
• Serum 3%

Chemical Compounds

• Fat 56%
• Heterogeneity 53%
• Mutation 48%
• Intraabdominal 39%
• High-Density Lipoprotein Cholesterol 30%
• Triglyceride 20%
• Protein 15%
• Metabolic 15%