Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins

Medicine & Life Sciences

• Prolidase Deficiency 100%
• Twins 57%
• Immunity 44%
• Phenotype 32%
• Telangiectasis 15%
• Interleukin-18 14%
• Skin 13%
• Mutation 10%
• proline dipeptidase 9%
• B-Lymphocytes 9%
• Therapeutics 8%
• Nonsense Codon 6%
• Lymphocyte Subsets 6%
• Splenomegaly 6%
• HLA-DR Antigens 6%
• Proline 6%
• Interleukin-17 6%
• Metabolic Diseases 6%
• Vasculitis 6%
• Regulatory T-Lymphocytes 5%
• Autoimmunity 5%
• High-Throughput Nucleotide Sequencing 5%
• Infections 5%
• Intellectual Disability 5%
• Sample Size 5%
• Lower Extremity 4%
• Genes 4%
• Collagen 4%
• Biopsy 3%
• Antibodies 3%
• Enzymes 3%
• Proteins 2%