EXTAN™ kits - Expert know-how at your fingertips

The ready-to-use primer set – reduces your turn around times and costs  

EXTAN™ will accelerate your diagnostic process. Primer design and testing is no longer necessary. On-site PCR/sequencing analyses with highly standardized and validated EXTAN™ primer sets will yield assured test results which can be subsequently analyzed using the EXTAN™ mutation database.  

Mutation database – get first-hand medical expertise  

The EXTAN™ mutation database is one of the world’s largest databases for genetic mutations. This tool will simplify the interpretation of identified mutations and will enable knowledge exchange with other experts.  

As a consequence, EXTAN™ will account for better understanding of your patient’s disease. Suggestions of how to treat rare diseases can be made faster and more precisely in the future – also based on the
detailed phenotype-genotype data being documented.  

Centogene is offering kit systems for many indications, among these are: Weill-Marchesani syndrome, metachromatic leukodystrophy, spastic paraplegia, glycogen storage disease II, Fabry disease, Charcot-Marie-Tooth disease, Niemann-Pick disease and Mast syndrome.

Knowledge transfer takes place through the supply of validated primer sets.