Genetic Testing for Renal Disorders

Detects genetic variants associated with progressive kidney disease and hearing loss.

Detects genetic variants associated with a multisystem disorder of renal and retinal abnormalities.

Detects genetic variants associated with hereditary renal tubulopathies causing renal salt loss

Detects genetic variants associated with ciliopathies affecting kidneys, brain, eyes and skeletal development

Detects genetic variants associated with cystic kidney diseases and progressive renal dysfunction

Detects genetic variants associated with hereditary hypomagnesemia and renal dysfunction.

Detects genetic variants associated with impaired water balance in the renal system, causing polyuria and polydipsia

Detects genetic variants associated with atypical hemolytic uremic syndrome and thrombotic microangiopathies

Detects genetic variants associated with hypophosphatemic rickets and skeletal deformities

Detects genetic variants associated with Joubert syndrome and multisystem neurodevelopmental disorder

Detects genetic variants associated with early-onset hereditary hypertension and abnormalities of renal sodium handling

Targeted NGS Gene Panel (Meckel Syndrome). Genes: B9D1, B9D2, CC2D2A, CEP290, KIF14, MKS1, NPHP3, RPGRIP1L, TCTN2, TMEM1

Detects genetic variants associated with inherited nephrolithiasis and nephrocalcinosis

Detects genetic variants associated with nephronophthisis and progressive kidney failure

Detects genetic variants associated with hereditary nephrotic syndrome and glomerular filtration barrier dysfunction

Detects genetic variants associated with polycystic kidney disease and progression to renal failure

Detects genetic variants associated with primary ciliary dyskinesia and chronic respiratory disease

Ανιχνεύει γενετικές παραλλαγές που σχετίζονται με πρωτοπαθή υπεροξαλουρία, νεφρολιθίαση και νεφρική βλάβη

Detects genetic variants associated with aldosterone resistance and electrolyte imbalance

Detects genetic variants associated with congenital kidney anomalies with risk of chronic kidney disease

Detects genetic variants associated with renal tubular acidosis and disorders of acid-base balance

Detects genetic variants associated with kidney dysfunction and progressive retinal degeneration