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PEDIATRICS & RARE DISEASES

Whole Genome Sequencing

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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. 

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

Whole Exome Sequencing

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

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

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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

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

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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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