Genetic Counseling

ISPD understands the unique perspective that Genetic Counselors (GCs) contribute, and considers them an integral part of the society and its purpose. The Genetic Counseling (GC) SIG was launched at the ISPD annual conference in Washington, DC in July 2015.

The SIGs mission is to encourage the exchange of information and experience among professionals providing genetic counseling as well as increasing international awareness of the profession.

SIG Topics of Discussion/Interest

  • Screening and diagnostic techniques
  • Chromosome analysis and microarray
  • Pan-Ethnic carrier screening
  • International collaboration among GCs
  • Genetic counselor training
  • International utilization of GCs
  • Development of an international database of prenatal GCs

Global Updates, August 2019

“The Art of Genetic Counseling in the Era of Genomic Testing” at ISPD 2019.

By Kelly Chen, MS and Katie Ellis, MS, Co-Chairs Genetic Counseling SIG

“How do I explain non-paternity in a tactful manner?”

“Should I discuss the potential impact of knowing about adult-onset diseases through prenatal microarray?”

How do I counsel a patient with an ongoing pregnancy (following mosaic embryo transfer) who will only consider noninvasive screening options?

Are these questions that you consider when counseling patients?  If they are, please join us in Singapore on Tuesday 10 September 2019 at the Genetic Counseling special interest group breakfast session of ISPD2019.  Everyone is welcome to attend as our expert speakers walk us through the challenges of pre-test counseling for complex genomic tests and share their experiences and strategies used when speaking to patients about the details of testing.


International Context-sensitive Practice in Prenatal Counseling and Clinical Practice 

Judith Jackson, on behalf of the Genetic Counselling and Ethics of Reproductive Testing and Fetal Therapy SIGs

The 2018 ISPD conference in Antwerp, Belgium hosted 609 people from all over the world representing 50 countries. The co-chairs of the Ethics and Genetic Counseling Special Interest Groups designed a highly successful pre-conference course that highlighted international variation in the utilization of prenatal screening and diagnostic technologies. Our speakers came from many disciplines, and each spoke about the clinical and regulatory landscape of prenatal services in their regions, including South America, China, the United Kingdom, Israel, and the United States. Highlights of each invited speaker are provided here, with further suggested reading.

Latin America – Socioeconomic and Legal Restrictions on Prenatal Testing

Prof Lucas Otaño, MD PhD, from Hospital Italiano in Buenos Aires, Argentina, discussed utilization of prenatal services in Latin America. Socioeconomic status impacts access to prenatal services in Argentina and the rest of Latin America as patients usually have to pay out-of-pocket for testing. In Argentina, this means than less than 1% of patients have noninvasive prenatal testing (NIPT) and there are no guidelines from scientific societies or public health organizations regarding the utilization of NIPT. Furthermore, pretest counselling before NIPT is very limited and Brazil is the only country in Latin America that has genetic counselors.

The other factor that impacts the availability of prenatal services in Latin America is the restricted availability of termination. In South America, Uruguay is the only country in which abortion is available without restrictions on indications. Although abortion is illegal in Argentina, approximately 400,000 women in Argentina have terminations annually. Death from termination is the most common cause of maternal mortality in Argentina. Despite this, Argentina’s senate recently rejected a bill to legalize abortion following a divisive public debate.

Further reading: Lucas Otaño & Laura Igarzábal (2015) Noninvasive Prenatal Testing for Fetal Aneuploidy in Argentina, AJOB Empirical Bioethics, 6:1, 111-114, DOI: 10.1080/23294515.2014.993439

China – Balancing Two-child Policy Reform with the Consequences of Advanced Maternal Age

Dong Dong PhD from the Hong Kong Baptist University, Hong Kong SAR, reviewed the tension between the quantity and the quality of human reproduction along a historical timeline in contemporary China. When China began its one-child policy, having one perfectly healthy baby meant granting the newborn certain economic, social and cultural prestige that could lead to a good start in the future global competition. “Winning at the starting line” became the most popular and powerful catchphrase for Chinese parents who autonomously internalized and acted upon the State’s will of having a “high-quality” population. However, when the two-child policy was initiated in 2016, it created a tension between encouraging more births overall, and encouraging more women over age 35 to have a second child, which in turn could cause an increase in the rate of birth defects. The National Health and Family Planning Commission repeatedly emphasized the prevention of birth defects as a “focal point” for the sake of “comprehensive two-child policy reform.” But, unlike a commodity, the “quality” of a baby can hardly be assured even through the strictest “quality inspection system.” Accordingly, the State has invented, adopted and utilized all types of political, economic, and social strategies to solve this dilemma between birth rate and genetic health. Dr. Dong also traced the historical change of prenatal genetic testing practices in China since the 1990s and revealed the significance that selective reproduction technologies could have in social, cultural and regulatory terms, and the role that they could play in shaping governance practice.

Suggested reading:  Jianfeng Zhu & Dong Dong. Chapter 7. From quality control to informed choice: Understanding “good birth” and prenatal genetic testing in contemporary urban China.

Gibbon, S. (Ed.), Prainsack, B. (Ed.), Hilgartner, S. (Ed.), Lamoreaux, J. (Ed.). (2018). Routledge Handbook of Genomics, Health and Society. London: Routledge.

United Kingdom – National Implementation of Publicly-funded NIPT and Controversy over Informed Choice

Ms Jane Fisher is Director of the UK Charity Antenatal Results and Choices (ARC). ARC provides independent non-directive information and support to women and couples through prenatal screening and its consequences. ARC works closely and collaboratively with professionals in the field and runs a well-established training program. Jane noted that the UK (with the exception of Northern Ireland) has a standardized prenatal screening program overseen by the UK National Screening Committee. All women accessing National Health Service (NHS) prenatal care (which is almost all pregnant women) are offered screening for trisomy 21, 18 and 13, for hemoglobinopathies and structural fetal anomalies. Screening for Down syndrome is hotly contested by advocates for people living with the condition and anti-choice campaigners, particularly in the era of cell-free DNA techniques. NIPT has been available and widely used in the private sector since 2012. The NHS are planning to implement the technology into the current trisomy screening program by the end of 2018. In preparation for this, a national training program for staff has been rolled out that included input from ARC, disability specific organizations and parents of affected children. The objective is to facilitate personal informed choice throughout screening and diagnosis. Abortion law in England, Scotland and Wales allows for terminations for serious fetal anomaly without gestational time limit. However, in practice very few terminations occur after the 24 week cut off for most abortions.   

For further information about Antenatal Results and Choices go to

United States – heterogeneity in prenatal care and reproductive choices

Marsha Michie PhD from Case Western Reserve University in Cleveland, Ohio, United States, spoke about the clinical landscape for prenatal care in the US. She noted that, because the practice of medicine in the US is regulated by individual states, an individual woman’s prenatal care may vary widely. The prenatal care she receives is shaped by where she lives, her income and insurance status, and any local idiosyncrasies of her health care provider. For example, California’s comprehensive prenatal screening program is inexpensive and well-supported by a statewide network of perinatal diagnostic clinics, staffed by genetic counselors and maternal-fetal medicine specialists. This program is fairly unique in the US, and many states have very few genetic counselors or perinatal specialists. In these places, prenatal care providers may rely on newer cell-free DNA screening because it is easy to access—but they also may have limited access to information about these tests beyond company-produced marketing materials. Abortion access also varies between states, and restrictions on abortion have increased markedly in the last several years. In 2017, 19 of the 50 states in the US enacted a total of 63 restrictions on abortion access. With impending changes to the US Supreme Court, access to legal abortion in many states may end altogether.

For more information on Dr Michies’ research, go to the Prenatal Information Research Consortium at

Israel – relative importance of reproductive carrier screening in prenatal care

Dr. Adi Reches, ObGyn and Medical Geneticist from the Tel Aviv Sourasky Medical Center spoke about the landscape of prenatal care and utilization in Israel. The Israeli Health Ministry funds prenatal genetic screening for common conditions for all citizens. The uptake is high among the secular population, due among other things to growing awareness of the treating ObGyns. Due to communities that tend to wed within themselves, specific pathogenic variants are also screened for, aimed at the relevant populations. Amongst religious Jews a program called Dor Yesharim screens both partners before matrimony, so that carriers of the same condition do not wed. Preimplantation genetic diagnosis is available and funded for carriers of genetic conditions.

All women are offered screening for trisomy 21 structural fetal anomalies via first and second trimester serum screening and ultrasound system scans. Amniocentesis is also funded for all women over 35, those at high risk for trisomy 21, or those at high risk for an affected fetus, as asserted by a medical geneticist. NIPT is available, currently as an out-of-pocket service, and is usually partly reimbursed by supplemental health care insurance.  The genetic society in Israel is currently trying to introduce NIPT as part of the funded screening tests in pregnancy. Abortion law in Israel allows for termination of pregnancies after approval from a committee up to 23 weeks. After this cutoff, a special committee can still approve of termination, but very serious fetal anomaly needs to be proven.

For more information on government recommendations for genetic testing in Israel, see

Case-based interactive roundtables

Following these invited presentations, the SIG attendees worked in small groups to discuss case scenarios common to their areas and to consider how approaches might differ. This allowed participants to learn more about international variation in the utilization of prenatal screening and to obtain a greater appreciation of the importance of social context in implementation of new technologies. For further information or to join the ethics or genetic counseling special interest groups, please contact Judith Jackson or Marsha Michie


SIG Leadership

Chair: Katie Ellis

Meeting Minutes

10 September 2019 - Singapore
11 July 2016 - Berlin, Germany (to be posted)
11 July 2016 - SIGs and Education Committee
15 July 2015 - Washington, DC USA (to be posted)

Annual Reports