Atypical hemolytic uremic syndrome (aHUS)
Our atypical hemolytic uremic syndrome panel includes genes used for the molecular diagnosis of this syndrome.
- TAT : 28 working days
- Sample : EDTA blood
Included Syndromes & Disorders
- Atypical hemolytic uremic syndrome
- Methylmalonic aciduria and homocystinuria
Nephro
Screening tool for prevalent hereditary kidney disorders and cilia dysfunction-related disorders, but it does not include PKD1 analysis.
- TAT : 28 working days
- Sample : EDTA blood
Included Syndromes & Disorders
- Alport syndrome
- Bardet-Biedl syndrome
- Bartter syndrome
- Combined pituitary hormone deficiency
- Focal segmental glomerulosclerosis
- Heterotaxy syndrome
- Hypogonadotropic hypogonadism
- Intrahepatic cholestasis
- Joubert syndrome
- Kallmann syndrome
- Leber congenital amaurosis
- Meckel syndrome
- Nephronophthisis
- Nephrotic syndrome
- Neonatal mitochondrial hepatopathies
- Polycystic kidney disease
- Pseudohypoaldosteronism
- Primary ciliary dyskinesia
- Renal tubular acidosis
- Renal tubular dysgenesis
- Skeletal dysplasia
- Skeletal ciliopathy
