Conditions / Syndrome
Alport syndrome 3A
info · Syndrome
An Alport syndrome that has_material_basis_in heterozygous mutation in the COL4A3 gene.
Signs and symptoms
- Proteinuria
- Microscopic hematuria
- Azotemia
- Glomerulonephritis
- Nephrocalcinosis
- Stage 5 chronic kidney disease
- Nephritis
- Anterior polar cataract
- Nephrotic syndrome
- Renal insufficiency
Also known as: autosomal dominant Alport syndrome 3A