Histopathology, ultrastructure, and clinical phenotypes in thin glomerular basement membrane disease variants

Keyphrases

• Alport 100%
• Alport Syndrome 16%
• Autosomal Recessive 16%
• Basement Membrane 83%
• Chronic Kidney Disease 16%
• Clinical Evidence 16%
• Clinical Phenotype 100%
• COL4A3 mutation 16%
• COL4A4 Gene 16%
• COL4A5 mutation 16%
• Collagen 16%
• Collagen III 33%
• Disease Variants 100%
• Electron Microscopy 16%
• End-stage Renal Disease 16%
• Family History 33%
• Genetic Studies 16%
• Glomerular Basement Membrane 100%
• Glomerulosclerosis 33%
• Glomerulus 16%
• Hematuria 50%
• Histologic 16%
• Hypertension 33%
• Intramembranous 16%
• Kidney Biopsy 16%
• Kidney Pathology 16%
• Lamellation 33%
• Lucency 16%
• Nephritis 66%
• Nephrotic-range Proteinuria 16%
• Patient Management 16%
• Progressive Renal Disease 16%
• Proteinuria 33%
• Renal Biopsy 16%
• Skin Biopsy 33%
• Skin Diagnostics 16%
• Ultrastructure 100%
• X-linked 16%

Medicine and Dentistry

• Alport Syndrome 20%
• Autosomal Recessive Inheritance 20%
• Basement Membrane 100%
• Chronic Kidney Disease 20%
• Collagen Type 3 40%
• Collagen Type 5 20%
• Diseases 100%
• Electron Microscopy 20%
• End Stage Renal Disease 20%
• Family History 40%
• Glomerulosclerosis 40%
• Glomerulus 20%
• Glomerulus Basement Membrane 100%
• Hematuria 60%
• Histopathology 100%
• Nephritic Syndrome 80%
• Nephropathy 40%
• Prematurity 40%
• Proteinuria 60%
• Renal Biopsy 40%
• Skin Biopsy 40%
• Ultrastructure 100%