Metabolik Disorders

Citrin Deficiency
Citrullinemia, type 1
Congenital Disorders of Glycosylation
Fatty Acid Oxidation Disorder
Glutaric Aciduria, type 1
Glutaric Aciduria, type 2
Glycogen Storage Disease
Hemochromatosis
Lysosomal Storage Disease
Metabolic Myopathy and Rhabdomyolysis
Methylmalonic Aciduria and Homocystinuria
Mucopolysaccharidosis 
NEW!!
Porphyria
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency
Smith Lemli Opitz Syndrome
Urea Cycle Disorder
Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency

Whole Exon Sequencing

Whole Genom Sequencing

Genetic Passport Metabolic Disorders selection consists of tests for molecular diagnostics of metabolic disorders. Metabolic disorders are highly diverse groups of conditions with variable severity of symptoms, commonly neurological impairment, organomegaly, and mental retardation are involved. The mode of inheritance is usually autosomal recessive but can also be X-linked.

The testing portfolio includes single gene tests as well as multigene panels. Glycogen and lysosomal storage diseases, fatty acid oxidation disorders, and urea cycle disorders are represented among others.

Confirmatory genetic testing allows effective treatment, genetic counseling, and risk assessment for family members.

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