Prenatal and Newborn Genetic Testing Market Expected to Achieve a Strong 8.5% CAGR, to Reach 15.2 USD Billion by 2035

WiseGuy Reports, Oct. 2025 (Press Release) – The Prenatal and Newborn Genetic Testing Market Global Outlook:

Global Prenatal and Newborn Genetic Testing Market Growth Analysis and Trends Report Test Type (Carrier Screening, Non-Invasive Prenatal Testing, Amniocentesis, Chorionic Villus Sampling), By Technology (Next-Generation Sequencing, Microarray Analysis, Polymerase Chain Reaction), By Application (Detect Genetic Disorders, Fetal Sex Determination, Anomaly Detection), By End Use (Hospitals, Diagnostic Laboratories, Research Institutions) and By Regions - Global Industry Forecast 2025 to 2035

Prenatal and Newborn Genetic Testing Market Overview

Prenatal and Newborn Genetic Testing Market Set to Witness Remarkable Growth by 2035

The Prenatal and Newborn Genetic Testing Market is experiencing rapid growth, fueled by technological advancements, regulatory approvals, and rising consumer awareness of genetic disorders. Valued at USD 6.16 billion in 2024, the market is expected to reach USD 6.69 billion in 2025 and expand to USD 15.2 billion by 2035, registering a CAGR of 8.5% over the forecast period. B2B stakeholders, including diagnostic laboratories, hospitals, research institutions, and biotechnology companies, are leveraging innovative testing solutions to provide early diagnosis and improved patient care.

Genetic testing for prenatal and newborn stages is increasingly being adopted to detect chromosomal abnormalities, single-gene disorders, and inherited conditions. Applications include screening for Down syndrome, cystic fibrosis, thalassemia, and other genetic diseases. Rising prevalence of genetic disorders, increasing healthcare expenditure, and growing awareness among parents and healthcare providers are driving market adoption.

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Advancements in testing technologies, such as next-generation sequencing (NGS), microarrays, PCR-based tests, and non-invasive prenatal testing (NIPT), are transforming the market. Companies are developing high-accuracy, cost-effective, and rapid testing platforms to improve diagnostic outcomes. Expansion of telehealth and remote testing services is further enabling wider access to genetic testing for prenatal and newborn care.

Regional Insights

North America dominates the Prenatal and Newborn Genetic Testing Market, driven by advanced healthcare infrastructure, high adoption of cutting-edge diagnostics, and robust research initiatives. The U.S. is a key contributor, with widespread implementation of prenatal screening programs and supportive government regulations. Europe holds a significant market share, backed by growing awareness, reimbursement policies, and stringent regulatory frameworks.

APAC is emerging as a high-growth region due to increasing population, rising healthcare expenditure, and expanding awareness about genetic disorders. Countries such as China, India, Japan, and South Korea are witnessing rapid adoption of advanced genetic testing solutions. South America and MEA show steady growth, fueled by healthcare investments, collaborations with global testing companies, and growing demand for early diagnostics.

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Market Segmentation

The Prenatal and Newborn Genetic Testing Market is segmented to provide actionable insights:

• Test Type: Non-invasive prenatal testing (NIPT), invasive prenatal testing, newborn screening tests, and carrier screening.
• Technology: Next-generation sequencing, PCR, microarrays, and other molecular diagnostics techniques.
• Application: Detection of chromosomal abnormalities, single-gene disorders, and inherited conditions.
• End Use: Hospitals, diagnostic laboratories, research institutions, and specialty clinics.
• Regional Analysis: North America, Europe, APAC, South America, and MEA.

Competitive Landscape

Key players in the Prenatal and Newborn Genetic Testing Market include Quest Diagnostics, Invitae, Gene by Gene, Illumina, Thermo Fisher Scientific, Agilent Technologies, Roche, Natera, PerkinElmer, Sequenom, ArcherDx, Genomic Health, Fulgent Genetics, Myriad Genetics, and Laboratory Corporation of America. These companies focus on innovation, strategic collaborations, product development, and geographic expansion to strengthen market presence and address the rising demand for early genetic testing.

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Market Opportunities

Opportunities in the Prenatal and Newborn Genetic Testing Market are substantial. Rising demand for early diagnosis, technological advancements in testing methods, expansion of prenatal screening programs, increased awareness of genetic disorders, and growth in telehealth and remote testing solutions are expected to drive market growth. Companies investing in integrated digital platforms, high-throughput testing, and patient engagement tools are likely to gain a competitive advantage.

Reasons To Buy The Prenatal and Newborn Genetic Testing Market Report:

➼ In-depth analysis of the Prenatal and Newborn Genetic Testing Market on the global and regional levels.

➼ Major changes in market dynamics and competitive landscape.

➼ Segmentation on the basis of type, application, geography, and others.

➼ Historical and future market research in terms of size, share growth, volume, and sales.

➼ Major changes and assessment in market dynamics and developments.

➼ Emerging key segments and regions

➼ Key business strategies by major market players and their key methods

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