Parameter | Method | Sample Type | Significance | |
---|---|---|---|---|
1 |
Congenital Adrenal Hyperplasia |
PCR |
Blood |
Discriminates between deletions, duplications and normal copy number status of the CYP21A2 gene in patients with CAH |
2 |
COPD/ AAT deficiency |
Multiplex PCR |
Blood |
Detects 'S and 'Z variants of the SERPINAI gene predisposing individuals to chronic obstructive pulmonary disease (CDPD) and liver disease due to deficiency to alpha-I antitrypsin (AAT) |
3 |
Congenital Adrenal Hyperplasia |
PCR-Hybridization |
Blood |
Testing for 1 1 CYP21A2 mutations |
4 |
Familial Mediterranean Fever |
PCR-Hybridization |
Blood |
Detection of 12 MEFV gene mutations |
5 |
Familial Mediterranean Fever |
PCR-Hybridization |
Blood |
Detection of 12 MEFV gene mutations and SAAI genotypes 1 .1 , 1 .3 and 1.5 |
6 |
Gaucher Disease |
PCR-Hybridization |
Blood |
Detection of 8 mutations and two recombinant alleles in the glucocerebrosidase (GBA) gene |
7 |
Alzheimer Disease |
PCR-Hybridization |
Blood |
Detection of isoforms Apo E2, E3 and E4 |