Hong Kong Med J 2025;31:Epub 28 Nov 2025
© Hong Kong Academy of Medicine. CC BY-NC-ND 4.0
COMMENTARY
The ethical dilemma of termination of pregnancy for minor fetal deformity
Shell F Wong, MB, BS, FHKAM (Obstetrics and Gynaecology)1,2; WL Lau, MB, BS, FHKAM (Obstetrics and Gynaecology)2,3
1 Private Fetal Maternal Medicine Practice, Hong Kong SAR, China
2 Department of Obstetrics and Gynaecology, The University of Hong Kong, Hong Kong SAR, China
3 Department of Obstetrics and Gynaecology, Kwong Wah Hospital, Hong Kong SAR, China
Corresponding author: Dr Shell F Wong (shellwong@hotmail.com)
One of the authors, during early clinical training,
encountered a 26-year-old pregnant woman admitted
to the labour ward with gross polyhydramnios in
early labour. She experienced rupture of membranes,
then presented with antepartum haemorrhage
and fetal distress. An emergency lower segment
caesarean section was arranged. Unfortunately,
her baby had trisomy 18. She experienced massive
haemorrhage, partly due to placental abruption
and polyhydramnios, resulting in disseminated
intravascular coagulation. She received more than
20 units of blood transfusion and required a total
hysterectomy.
In the 1990s, ultrasound machines were
not widely available in most obstetric units.
Frequently, we encountered mothers delivering
babies with lethal conditions such as anencephaly,
renal agenesis, lethal skeletal dysplasia, Edwards
syndrome, or Patau syndrome in the delivery suite.
This was a very distressing experience for the
mothers, their partners, family members, and the
attending obstetricians. When morphology scans
were introduced, it became a rewarding experience
for parents and clinicians because these lethal
conditions could be detected earlier. Early detection
allowed termination of pregnancy, reduced maternal
morbidity, and prevented distressing experiences for
both parents and attending staff.
As ultrasound resolution improved,
more treatable but serious conditions such as
diaphragmatic hernia, congenital heart disease,
gastroschisis, exomphalos, and fetal bowel
obstruction were detected. In large countries (eg, the
United States, the United Kingdom, and Australia),
prenatal detection of these congenital malformations
allowed in utero transfer to tertiary centres with
qualified neonatologists and paediatric surgeons,
who could provide appropriate and timely neonatal
resuscitation. This substantially reduced neonatal
morbidity and, in some cases, neonatal mortality.
On one hand, prenatal diagnosis enables
early detection and in utero medical or surgical
intervention. The clinical outcomes of Rhesus
isoimmunisation and twin-to-twin transfusion
syndrome have greatly improved with in utero blood transfusion and laser ablation of placental vessels.
Other conditions, such as congenital diaphragmatic
hernia, aortic stenosis, and spina bifida, have also
shown improved outcomes with prenatal treatment.
In these situations, physicians look through the
pregnant woman to the fetus and regard the fetus
as a distinct patient.1 On the other hand, overly
aggressive treatment may result in long-term
morbidity in the surviving child.2
As pregnant mothers and families have
become more receptive to termination of pregnancy,
the detection of babies with clinically significant
disabilities allows parents the option to discontinue
the pregnancy. Termination is often offered to
parents expecting babies with Down syndrome or
spina bifida, and screening for these conditions has
become routine in clinical practice.
With higher-resolution ultrasound machines,
specialists can now detect minor fetal deformities
such as microtia, syndactyly, oligodactyly,
polydactyly, and other small defects, including
minor ventricular septal or muscular septal defects.
In recent years of private practice, there has been an
increasing number of couples concerned about such
minor deformities, likely due to greater awareness
through social media and internet blogs. There is
also a growing willingness to terminate pregnancies
involving minor deformities, including cleft lip,
microtia, oligodactyly, and minor correctable heart
lesions.3 4 5 6
Sometimes, prenatal detection of conditions
such as transposition of the great arteries or an
aortopulmonary window can improve clinical
outcomes. It is, however, frequently disappointing
to find that parents decide to terminate these
pregnancies because they cannot accept the presence
of a large mediastinal scar or the small risk of serious
complications associated with major cardiac surgery.
As medical professionals, we have an obligation
to counsel such couples before termination of
pregnancy. Many of these abortions involve minor
deformities and occur close to the time of viability. A
number of couples choose termination because they
feel they can only accept a ‘perfect child’. For these
parents, in their view, the morphology scan must be ‘perfectly normal’. When minor or major deformities
are detected, the perceived solution is to terminate
the ‘imperfect child’. Termination of pregnancy is
legal under two circumstances: (1) if continuation
of the pregnancy would involve greater risk to
the life, physical, or mental health of the pregnant
woman than termination; and (2) if the child to be
born would be severely handicapped due to physical
or mental abnormality.7 Many terminations for
minor fetal anomalies are justified on the grounds of
maternal mental health. To reduce potential misuse,
psychological assessment should be considered.
Most gynaecologists agree to perform
termination of pregnancy out of respect for maternal
autonomy. Many obstetricians also support this
option, given that it is less likely to result in subsequent
medicolegal issues. Some fetuses with minor defects
may have underlying genetic disorders that cannot be
detected prenatally. Various reasons have been cited
by couples who choose termination for minor fetal
defects, including negative perceptions of disability,
cultural biases against disabled individuals, social
stigmatisation, intense societal competition, and
high parental expectations.3 8 9 10 Gynaecologists
treating these women should be reminded that false-positive
findings can occur, ranging from 1% to 9%
according to different reports.11 12 The false-positive
rate in prenatal ultrasound is not insignificant;
such misdiagnoses cause psychological distress for
parents and lead to over-medicalisation of both the
pregnancy and the child.
With advances in cosmetic and reconstructive
surgery, many minor deformities can now be
corrected to achieve near-normal and aesthetically
acceptable results.13 14 15 16 17 18 19 20 Thus, before deciding on
termination of pregnancy, couples should be
counselled by appropriate specialists, including ENT
(ear, nose, and throat) and plastic surgeons, as well
as other relevant subspecialists. These experts can
provide up-to-date information regarding surgical
outcomes, which may help reduce anxiety and
prevent unnecessary terminations based solely on
external appearance. Furthermore, with advances in
molecular genetics, many genetic syndromes can now
be confidently excluded, thereby alleviating anxiety
for both parents and attending obstetricians.21 22 23 24
In Hong Kong, legal abortion is permitted
only before 24 weeks of gestation.7 In many
countries, including the United Kingdom and
France, termination after 24 weeks is allowed when
two doctors agree that there is a serious threat to
the pregnant person’s life or in cases of severe fetal
disability.25 Similar practices could be considered in
Hong Kong to allow more time for investigations
and for couples to reflect carefully before making a
decision about abortion. To prevent misuse, however,
clearly defined indications should be established.
Practitioners who care for pregnant women face dilemmas when patients exercise autonomy
in ways that may result in adverse or unfavourable
outcomes for their babies or fetuses. Many ethicists
characterise such situations as maternal–fetal
conflicts. In conflict-based models, maternal rights
are viewed as conflicting with fetal rights, or moral
obligations owed to pregnant women are considered
in opposition to those owed to their fetuses.
Invoking the Hippocratic dictum “Do good, or at
least do no harm” as the physician’s primary moral
obligation, it can be argued that beneficence toward
the patient always overrides respect for autonomy.
Thus, prioritising beneficence toward the fetus may,
in effect, override not only respect for the pregnant
woman’s autonomy but also beneficence toward her.
This commentary aims to stimulate further
debate among medical professionals, legal
practitioners, and lawmakers. Should parents have
full autonomy to terminate a pregnancy for all minor
fetal defects? Do gynaecologists have the right to
refuse to perform such procedures? How should
the medical profession responsibly address this
issue? Should legislation permit late termination of
pregnancy beyond 24 weeks?
Author contributions
Both authors drafted the manuscript, approved the final
version for publication, and takes responsibility for its
originality, accuracy and integrity. Both authors had full
access to the data, contributed to the study, approved the final
version for publication, and take responsibility for its accuracy
and integrity.
Conflicts of interest
Both authors have disclosed no conflicts of interest.
References
1. Daffos F. Access to the other patient. Semin Perinatol 1989;13:252-9.
2. Chervenak FA, McCullough LB. Perinatal ethics: a
practical method of analysis of obligations to mother and
fetus. Obstet Gynecol 1985;66:442-6.
3. Lau WL, Hui EC, Lai FK, et al. Ethical discussion:
termination of pregnancy after prenatal diagnosis of cleft
lip in a Chinese population in Hong Kong. Hong Kong J
Gynaecol Obstet Midwifery 2023;13:74-80.
4. Guyot A, Soupre V, Vazquez MP, et al. Diagnostic
anténatal des fentes labiales avec ou sans fente palatine:
étude rétrospective et revue de la littérature [in French]. J
Gynecol Obstet Biol Reprod (Paris) 2013;42:151-8. Crossref
5. Hager C. Termination of pregnancy with a prenatal
diagnosis of cleft lip: cultural differences and ethical
analysis. Plast Surg Nurs 2002;22:24-8. Crossref
6. Cheng LR. Asian-American cultural perspectives on birth
defects: focus on cleft palate. Cleft Palate J 1990;27:294-
300. Crossref
7. Family Health Service, Department of Health, Hong Kong
SAR Government. Termination of pregnancy. Feb 2016.
Available from: https://www.fhs.gov.hk/english/health_info/woman/15673.html. Accessed 13 Nov 2025.
8. Berk NW, Cooper ME, Liu YE, Marazita ML. Social
anxiety in Chinese adults with oral-facial clefts. Cleft
Palate Craniofac J 2001;38:126-33. Crossref
9. Chan RK, McPherson B, Whitehill TL. Chinese attitudes
toward cleft lip and palate: effects of personal contact. Cleft
Palate Craniofac J 2006;43:731-9. Crossref
10. Hunt O, Burden D, Hepper P, Johnston C. The psychosocial
effects of cleft lip and palate: a systematic review. Eur J
Orthod 2005;27:274-85. Crossref
11. Debost-Legrand A, Laurichesse-Delmas H, Francannet C,
et al. False positive morphologic diagnoses at the anomaly
scan: marginal or real problem, a population-based cohort
study. BMC Pregnancy Childbirth 2014;14:112. Crossref
12. Vaughan J. ‘Misplaced faith’ in the 20-week morphology
scan. O&G Magazine. Winter 2009. Available from:
https://www.ogmagazine.org.au/11/2-11/misplaced-faith-in-the-20-week-morphology-scan/. Accessed 5 Feb 2025.
13. Zaputović S, Medić N. Surgically correctable congenital
fetal anomalies: ultrasound diagnosis and management.
Donald School J Ultrasound Obstet Gynecol 2016;10:338-49. Crossref
14. Bhatti SL, Daly LT, Mejia M, Perlyn C. Ear abnormalities.
Pediatr Rev 2021;42:180-8. Crossref
15. Chang CS, Bartlett SP. Deformations of the ear and their
nonsurgical correction. Clin Pediatr (Phila) 2019;58:798-805. Crossref
16. Siegert R, Magritz R. Otoplasty and auricular
reconstruction. Facial Plast Surg 2019;35:377-86. Crossref
17. Perenack J, Haggerty C, Webb D, Will M. Facial cosmetic
surgery. J Oral Maxillofac Surg 2017;75:e302-23. Crossref
18. Steinberg B, Caccamese J Jr, Costello BJ, Woerner J.
Cleft and craniofacial surgery. J Oral Maxillofac Surg
2017;75:e126-50. Crossref
19. Steinberg B, Caccamese J Jr, Padwa BL. Cleft and
craniofacial surgery. J Oral Maxillofac Surg 2012;70(11
Suppl 3):e137-61. Crossref
20. Fisher DM, Sommerlad BC. Cleft lip, cleft palate, and
velopharyngeal insufficiency. Plast Reconstr Surg
2011;128:342e-60e. Crossref
21. Westenius E, Conner P, Pettersson M, et al. Whole-genome
sequencing in prenatally detected congenital
malformations: prospective cohort study in clinical setting.
Ultrasound Obstet Gynecol 2024;63:658-63. Crossref
22. Petrovski S, Aggarwal V, Giordano JL, et al. Whole-exome
sequencing in the evaluation of fetal structural anomalies:
a prospective cohort study. Lancet 2019;393:758-67. Crossref
23. Qin Y, Yao Y, Liu N, et al. Prenatal whole-exome sequencing
for fetal structural anomalies: a retrospective analysis of
145 Chinese cases. BMC Med Genomics 2023;16:262. Crossref
24. Lord J, McMullan DJ, Eberhardt RY, et al. Prenatal exome
sequencing analysis in fetal structural anomalies detected
by ultrasonography (PAGE): a cohort study. Lancet
2019;393:747-57. Crossref
25. Dommergues M, Benachi A, Benifla JL, des Noëttes R,
Dumez Y. The reasons for termination of pregnancy in the
third trimester. Br J Obstet Gynaecol 1999;106:297-303. Crossref

