Metabolic disease gene panels

Metabolic disease gene panels

Hereditary metabolic diseases are hereditary disorders that occur in the synthesis and catabolism of proteins, carbohydrates and fats. Metabolic metabolic diseases can come into conflict with very different clinical findings that concern all systems. With the new generation of sequencing technology, appropriate and effective treatment process will be initiated. Hereditary metabolic diseases are classified under the following headings:

1-Lysosomal Storage Diseases

2-Glycogen Storage Diseases

3-Purine and Pyrimidine Diseases

4-Peroxisomal Diseases

5-Oxidation Disorders in Fat Acid

6-Mitochondrial Diseases

7-Carbohydrate Metabolism Diseases.

For the diagnosis and interpretation of metabolic diseases, POLGEN offers its own approach and genomic solution methods.

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