Rapid Genetic Diagnosis for Critically Ill Newborns

Baby Wolf: Rapid Genetic Diagnosis for Newborns

About

Medialthea supports A.B.C. Associazione per i Bambini Chirurgici del Burlo in strengthening advanced genetic diagnostics for critically ill newborns treated at the IRCCS Burlo Garofalo, a national reference center for maternal and child health.

The program focuses on enabling rapid genomic diagnosis for newborns born with, or presenting, severe and complex clinical conditions, allowing life-saving decisions to be made within the very first days of life.

Donate Now

Surgery Department of the IRCCS Maternal and Child Health Institute Burlo Garofolo

Main focus areas of the program

Rapid Genetic Diagnosis for Critically Ill Newborns

The program supports BABY WOLF, an advanced rapid genomic analysis pathway designed to drastically shorten diagnostic times for newborns in critical condition.

For critically ill newborns, time is a decisive factor:
a delayed diagnosis can mean missed therapeutic windows, irreversible neurological damage, or loss of life.

Medialthea’s support has contributed to:

Rapid genomic diagnosis for critically ill newborns
Early access to targeted therapies and precision medicine
Reduction of diagnostic uncertainty for families and clinicians
Integration of advanced bioinformatics into neonatal care
Strengthening national reference centers for rare pediatric diseases

Thanks to this support, it is now possible to overcome the limitations of traditional genetic testing, which can take weeks or even months, forcing clinicians to rely on non-specific or temporary treatments while families remain without clear answers.

Partners:

LEARN MORE ABOUT ABC BURLO

Latest updates on the project

Donate Now

Ensure excellent medical care, alongside emotional and personal support to children and their families.

IBAN MC5811999000010181539000192

Donations are made via bank transfer to the following IBAN, specifying the name of the program you wish to support as the payment reference.