Test Catalog

Hypercholesterolemia and hyperlipoproteinemia
€1,250.00 Laboratory:
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Nephronophthisis
€1,700.00 Laboratory:
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NPHP1 deletion/duplication analysis (MLPA)
€350.00 Laboratory:
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Nephronophthisis (NGS Panel)
€1,250.00 Laboratory:
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Cystic kidney disease
€2,950.00 Laboratory:
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PKD1/PKD2 sequencing parallel with NGS-panel
€1,400.00 Laboratory:
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Cystic kidney disease (NGS panel)
€1,250.00 Laboratory:
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Renal tubular dysgenesis
€950.00 Laboratory:
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Renal dysplasia, renal agenesia, CAKUT.
€1,400.00 Laboratory:
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Nephrotic syndrome
€1,400.00 Laboratory:
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Focal segmental glomerulosclerosis
€1,400.00 Laboratory:
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Alport syndrome and disorders of glomerular basement membrane (GBM)
€950.00 Laboratory:
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C1q deficiency
€950.00 Laboratory:
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Renal tubular acidosis
€950.00 Laboratory:
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Bartter syndrome and differential diagnoses
€1,250.00 Laboratory:
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Hypophosphatemic rickets
€1,250.00 Laboratory:
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Pseudohypoaldosteronism.
€950.00 Laboratory:
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Diabetes insipidus, nephrogenic.
€950.00 Laboratory:
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Hyperoxaluria
€950.00 Laboratory:
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Atypical hemolytic uremic syndrome and differential diagnoses
€1,250.00 Laboratory:
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Primary inherited aminoacidurias.
€950.00 Laboratory:
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Branchiootorenal syndrome
€950.00 Laboratory:
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Bardet-Biedl syndrome
€1,400.00 Laboratory:
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Joubert syndrome
€1,400.00 Laboratory:
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Meckel syndrome
€1,250.00 Laboratory:
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Senior-Loken syndrome
€1,250.00 Laboratory:
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Cholestasis familial
€950.00 Laboratory:
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Hypercholanemia and bile acid synthesis defects
€1,250.00 Laboratory:
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Impairment of the transport in hepatocytes and cholangiocytes
€950.00 Laboratory:
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Impairment of the organo morphogensis
€1,250.00 Laboratory:
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Test Catalog

Hypercholesterolemia and hyperlipoproteinemia

Nephronophthisis

NPHP1 deletion/duplication analysis (MLPA)

Nephronophthisis (NGS Panel)

Cystic kidney disease

PKD1/PKD2 sequencing parallel with NGS-panel

Cystic kidney disease (NGS panel)

Renal tubular dysgenesis

Renal dysplasia, renal agenesia, CAKUT.

Nephrotic syndrome

Focal segmental glomerulosclerosis

Alport syndrome and disorders of glomerular basement membrane (GBM)

C1q deficiency

Renal tubular acidosis

Bartter syndrome and differential diagnoses

Hypophosphatemic rickets

Pseudohypoaldosteronism.

Diabetes insipidus, nephrogenic.

Hyperoxaluria

Atypical hemolytic uremic syndrome and differential diagnoses

Primary inherited aminoacidurias.

Branchiootorenal syndrome

Bardet-Biedl syndrome

Joubert syndrome

Meckel syndrome

Senior-Loken syndrome

Cholestasis familial

Hypercholanemia and bile acid synthesis defects

Impairment of the transport in hepatocytes and cholangiocytes

Impairment of the organo morphogensis