Conditions / Genetic
nephrotic syndrome type 26
info · Genetic
A familial nephrotic syndrome characterized by onset of proteinuria in the first months or years of life that has_material_basis_in homozygous or compound heterozygous mutation in the LAMA5 gene on chromosome 20q13.
Signs and symptoms
- Nephrotic syndrome
- Focal segmental glomerulosclerosis
- Steroid-resistant nephrotic syndrome
- Stage 5 chronic kidney disease
Also known as: NPHS26