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

Keyphrases

• Activation Markers 10%
• Autoinflammatory 10%
• Cell Class 10%
• Class-switched Memory B Cells 10%
• Dysmorphic Features 20%
• Facial Telangiectasia 10%
• Immunological Abnormalities 10%
• Immunological Characteristics 100%
• Immunological Profile 10%
• Inflammatory State 10%
• Lymphocyte Subset Analysis 10%
• Multisystem Disease 10%
• PEPD Gene 20%
• Premature Stop Codon 10%
• Primary Antibody Deficiency 10%
• Prolidase 10%
• Prolidase Deficiency 100%
• Skin Ulcer 30%
• Telangiectasia 10%
• TEM Cell 40%
• Th1-Th2 10%
• Th17 Profile 10%

Medicine and Dentistry

• Dysmorphic Feature 20%
• Facies 10%
• Humoral Immune Deficiency 10%
• Interleukin 18 20%
• Memory B Cell 20%
• Paroxysmal Extreme Pain Disorder 20%
• Prolidase Deficiency 100%
• Proline Dipeptidase 10%
• Skin Ulcer 30%
• Stop Codon 10%
• Telangiectasia 20%

Immunology and Microbiology

• Atopy 25%
• Autosomal Recessive Inheritance 25%
• Follicular B Helper T Cells 25%
• Humoral Immune Deficiency 25%
• Lower Limb 25%