Miroslav Šašinka, Katarína Furková
Focal segmental glomerulosclerosis – hereditary forms
Focal segmental glomerulosclerosis (FSGS) is nephropathy with serious prognosis and complicated genetic and nongenetic
etiopathogenesis. Clinically FSGS is characterized with high steroid resistant proteinuria, nephrotic syndrome
evaluation, generalized oedema, hypoalbuminemia, hyperlipidaemia, serious hypertension and progressive renal function
worsening. FSGS is podocytopathy (disease of the podocytes), diagnosis is confirmed by renal biopsy. Genes in
FSGS regulate metabolism of the podocytes and its structure (cytoskeleton). Authors analyze the genetic regulation
of the primary and secondary FSGS, autosomal recessive and autosomal dominant familiar FSGS, they stress the most
known FSGS genes in this time and only briefly write about clinical symptoms, therapy and prognosis.