PEDIATRICS & RARE DISEASES

Whole Genome Sequencing

Recommended for complex pediatric cases, it analyses also the non-coding part of DNA - the part where there is no direct link to protein codification. 

It therefore analyses the interaction between the coding part of DNA and its errors in trascribing proteins.

Whole Exome Sequencing

Recommended for the study of any type of congenital disease. It covers 99% of the 4,500 genes known to be associated with diseases. 

Genando gets to a diagnosis in 65% of cases compared to 35% average in the market.

This test requires an accurate description of the personal and family's clinical picture. It is carried out on a blood test and results are available in 4 weeks.

SNP / CGH Array

This test is recommended in cases of congenital malformations or intellectual disabilities. 

It is carried out with a blood test of the patients and the parents. The results are available in approximately 20 days. 

Contact Us

Email: info@genando.com

Phone: +39-055-674100

Address

Genando s.r.l.

Via Mannelli 15r (interno 9r)

P.I.:06788020482

Aut.Comune di Firenze Provv. Dir.2019/DD/02831 del 05.04.2019

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