The demand for Mendelian Disorders testing in the United States has been steadily increasing, reflecting a growing recognition of the significance of genetic testing in healthcare. Mendelian Disorders, also known as monogenic disorders, are caused by mutations in a single gene and often have a clear inheritance pattern. This market demand surge can be attributed to various factors, including advancements in genetic testing technologies, heightened awareness of the role of genetics in health, and an increasing prevalence of Mendelian Disorders within the population.
Advancements in genetic testing technologies have played a pivotal role in driving the demand for Mendelian Disorders testing in the US. The field of genomics has witnessed remarkable progress, with the development of high-throughput sequencing technologies, such as next-generation sequencing (NGS). These technologies enable comprehensive analysis of an individual's genetic makeup, allowing healthcare professionals to identify specific gene mutations associated with Mendelian Disorders more efficiently and accurately. As the cost of genetic testing continues to decrease, it has become more accessible to a broader range of individuals, contributing to the growing demand for Mendelian Disorders testing.
There has been a notable increase in public awareness regarding the role of genetics in determining health outcomes. This heightened awareness is driven by factors such as increased media coverage of genetic discoveries, educational initiatives, and the growing popularity of direct-to-consumer genetic testing services. As individuals become more informed about the potential genetic underpinnings of certain health conditions, there is a corresponding increase in demand for Mendelian Disorders testing to assess and understand their own genetic risk factors.
The prevalence of Mendelian Disorders within the population has also contributed significantly to the rising demand for testing services. With an increasing understanding of the genetic basis of various diseases, healthcare professionals are better equipped to identify individuals at risk of Mendelian Disorders and provide targeted genetic testing. This proactive approach to healthcare, focusing on early identification and intervention, has driven the demand for testing services to prevent or manage these disorders effectively.
The US Mendelian Disorders testing market is witnessing a surge in the development and availability of genetic testing panels tailored to specific disorders. These panels allow for the simultaneous analysis of multiple genes associated with a particular Mendelian Disorder, streamlining the testing process and providing comprehensive insights. This trend is especially crucial for conditions with overlapping symptoms, enabling more accurate and timely diagnoses.
In addition to traditional healthcare settings, the demand for Mendelian Disorders testing has extended to research and pharmaceutical sectors. Genetic testing plays a vital role in the identification of potential therapeutic targets and the development of personalized medicine. The collaboration between research institutions, pharmaceutical companies, and genetic testing laboratories has fueled innovation and expanded the scope of Mendelian Disorders testing applications.
As the demand for Mendelian Disorders testing continues to rise, there is a growing emphasis on genetic counseling services to support individuals and families in understanding and interpreting their test results. Genetic counselors play a crucial role in helping individuals make informed decisions about their healthcare based on their genetic information, contributing to a more comprehensive and patient-centered approach to genetic testing.
Mendelian Disorders Testing Market Size was valued at USD 0.4 billion in 2023. The Mendelian Disorders Testing Market industry is projected to grow from USD 0.43 billion in 2024 to USD 0.96 billion by 2032, exhibiting a compound annual growth rate (CAGR) of 8.54% during the forecast period (2024 - 2032). Genetic testing involves the use of laboratory methods to study the genes inherited from mother or father. These tests may be used to identify increased risks of health problems, to diagnose the mutations in the genes, to choose treatments, or to assess responses to treatment.
Mendelian disorders also known as monogenic diseases arise due to the modifications in a single gene occurring in all cells of the body. Currently, it is estimated that over 10,000 of human diseases are known to be monogenic. These disorders are responsible for a heavy loss of life. The global prevalence of monogenic diseases at birth is approximately 10 in every 1000 infants.
The Mendelian disorders are caused by a single mutated gene which can be present on single or both chromosomes. Both females and males are equally affected by this disorder. Sickle cell anemia, Cystic fibrosis, Tay-Sachs disease, SCID, Gaucher's disease, Huntington's disease, neurofibromatosis, thalassemia, polycystic kidney disorder, and familial hypercholesterolemia are some of the common monogenic disorders. Nowadays, there are several tests performed to treat monogenic disorders such as diagnostic testing, carrier testing, predictive & pre-symptomatic testing, prenatal testing and new-born screening.
The carrier testing is a type of genetic testing that is used to determine a carrier person for monogenic disorders. Having said that, more and more genetic tests are being developed for a lot of other genetic disorders. Oncology segment has been the major focus area of the companies developing these tests as the large pool of population is affected by this fatal disease. The continuous rise in the prevalence of the genetic disorders has boosted the growth of the genetic testing market.
Intended Audience
The Mendelian disorders testing market is segmented on the basis of test type, disorder type, and end-user.
On the basis of the test type, the Mendelian disorders testing market is segmented into carrier testing, diagnostic testing, new-born screening, predictive & pre-symptomatic testing, prenatal testing, and others
On the basis of the disorder type, the mendelian disorders testing market is segmented into cystic fibrosis, sickle cell anemia, severe combined immunodeficiency (SCID), Tay-Sachs disorder, polycystic kidney disorder, Gaucher's disease, Huntington's disease, neurofibromatosis, thalassemia, familial hypercholesterolemia, and others
On the basis of the end user, the mendelian disorders testing market is segmented into hospitals, ambulatory surgical centers (ASCs), and specialized clinics.
The Mendelian disorders testing market is segmented as the Americas, Europe, Asia Pacific and the Middle East and Africa.
The Americas is projected to hold the largest share of the mendelian disorders testing market. The unique opportunity drives the Mendelian disorders testing the market, and the focused issues stress on the need for more research on monogenic disorder tests. In the United States, sickle cell anemia affects around 72,000 people, the majority of this population have their ancestors from Africa. All the factors above are anticipated to boost the market growth in the U.S. and ensure its dominance over the forecast period.
Europe is expected to capture the second lead in this market in the coming five years owing to substantial technological advancements. About 6,000 people are affected with hemophilia in the UK. Moreover, about 5400 people in the U.K with hemophilia A and about 1100 with hemophilia B.
The market in the Asia Pacific is expected to witness the fastest growth rate due to increasing prevalence of monogenic disorders throughout the globe, which will boost the growth of the monogenetic disorders testing market.
The Middle East and Africa are also expected to show healthy growth in the coming five years.
The existing players are strengthening their foothold in the industry by introducing technologically advanced products. Regulatory bodies such as the US FDA and the European CE mark, although stringent, are approving equipment that fulfills all clinical data requirement and other safety criteria.
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