BabyNext

About the test

BabyNEXT is a genetic test that analyzes certain hereditable conditions that can appear soon after birth or later in childhood. BabyNEXT is able to screen for a wider range of conditions than current newborn screening.

Brochure for future parents

WHY CHOOSE BabyNEXT

Complete test

Complete test

BabyNEXT is able to screen for a wider range of conditions than newborn screening available.

Early diagnosis

Early diagnosis

BabyNEXT allows the early screening of conditions that may not be discovered until symptoms appear.

Targeted therapy

Targeted therapy

BabyNEXT can help to know whether to take proactive steps, sooner, to care for baby’s health.

How it works

Groundbreaking technologies

BabyNEXT is performed starting from a buccal swab, from which the baby’s DNA is extracted. Our expert laboratory technicians analyze the baby’s genes for more than 200 conditions by using the advanced NGS (Next Generation Sequencing) technology.


Groundbreaking technologies

BabyNEXT

guarantees competence, experience and quality
Personalized

Personalized

It includes a pharmacogenetic analysis of a child’s response to more than 30 medications that may be prescribed, during childhood, thus allowing a personalize treatment throughout life.

Comprehensive

Comprehensive

It detects 200+ childhood conditions to give more comprehensive insight into baby’s health.


Actionable

Actionable

It includes only conditions that may be treated with medication, dietary modification, or other therapies.


Advanced

Advanced

It utilizes a groundbreaking sequencing technology (NSG), coupled with a leading bioinformatic analysis.


Useful

Useful

It helps parents and pediatrician to know whether to take proactive steps, sooner, to care for baby’s health.

Non-invasive

Non-invasive

A simple cheek swab is designed for gentle and simple non-invasive sample collection.

Accurate

Accurate

Sensitivity and specificity >99%.

Fast

Fast

Turnaround time of just 15 days.

Levels of screening

2 levels of screening

STANDARD

Screens for more than
80 diseases
including 34 conditions of the Recommended Uniform Screening Panel RUSP

Genes Investigated



Both BabyNEXT screen levels allow to evaluate the baby response to more than 30 medications, thus allowing a personalized treatment throughout life.

EXTENDED

Screens for more than
200 diseases
including 34 conditions of the Recommended Uniform Screening Panel RUSP

Genes Investigated

BabyNEXT

Indication for testing

Individuals presenting symptoms of a metabolic disorder

Individuals with a positive family history of metabolic disease.

Individuals without a positive family history but with symptoms resembling the specific disease indication.

Individuals with a negative, but suspected, family history in order to perform proper genetic counselling.

Useful documents

Brochures and forms

BabyNEXT Brochures

Brochure for future parents

BabyNEXT Brochure
for future parents

Brochure for physicians

BabyNEXT Brochure
for physicians

BabyNEXT Useful Forms

Modulo di richiesta esame BabyNEXT

BabyNEXT
Requisition Form

BabyNEXT Patient Information

BabyNEXT
Patient Information

Informed consent

BabyNEXT
Informed consent

Technical report

BabyNEXT EXTENDED
Technical report

Technical report

BabyNEXT STANDARD
Technical report

BabyNEXT Kit instructions buccal swab

BabyNEXT
Buccal swab kit instructions

BabyNEXT

Simple procedure and fast reporting

ORDER the DNA collection kit that will be sent directly to your office or center.

FILL-IN all required TRF information and enclose the informed consent

COLLECT a DNA sample through a buccal swab performed on the child.

SHIP the sample to Genoma Lab (no shipping costs)

RECEIVE the results in 15 working days.

IN CASE OF A POSITIVE RESULT WE RECOMMEND TO REQUEST A COUNSELING WITH A SPECIALIST IN GENETICS

CONTACT US

Information request form

Information request

Contact us by calling the Contact Center 06.164161500 (12 lines PBX ) to discover how you can perform BabyNEXT test or fill out the form below. Your personal information will be used exclusively to satisfy your request, in the absolute respect of your privacy.

I have already performed prenatal exams at Genoma Lab
I have read and accept Privacy Policy  

ROME Laboratories
Via Castel Giubileo, 11
00138 Rome (RM)
Contact center: + (39) 06.164161500 (12 lines PBX)
Fax : +(39) 06.64492025

MILAN Laboratories
Via Enrico Cialdini, 16 (Affori Centre)
20161 Milan (MI)
Contact center: + (39) 06.164161500 (12 lines PBX)
Fax : + (39) 02 39297627

E-mail
info@laboratoriogenoma.eu

Website
http://www.laboratoriogenoma.eu

Copyright © 2017 EUROFINS Genoma Group Srl a socio unico - All rights reserved | P.Iva 05402921000 | Privacy Policy | Cookie Policy