What Causes Craniosynostosis During Pregnancy?
At a Glance
Craniosynostosis during pregnancy is a natural developmental event, not caused by a mother's diet, stress, or habits. It is most often caused by a complex biological misfire, spontaneous genetic changes (de novo mutations), or physical crowding in the womb known as intrauterine constraint.
In this answer
3 sections
The most important thing you need to know is this: you did not cause your baby’s craniosynostosis. It is completely natural to feel guilty and wonder if your diet, sleep position, or stress levels during pregnancy are to blame, but medical research is clear that these daily choices do not cause the skull’s sutures to fuse early. For the vast majority of babies, especially those with isolated (non-syndromic) craniosynostosis, this is simply a developmental hiccup—a complex biological event that occurred as your baby was forming [1][2].
The Biology of a “Developmental Hiccup”
Most babies diagnosed with this condition have non-syndromic craniosynostosis, meaning the early fusion of the skull suture is the only issue and is not part of a broader genetic syndrome [3]. Medical experts recognize this isolated form as a complex developmental defect [1]. As the fetus develops, intricate chemical signals tell the body how to grow. Sometimes these signals misfire, causing the skull bones to fuse improperly [4]. This is an unpredictable process influenced by a mix of subtle genetic predispositions and the biological environment of the womb, completely unrelated to your everyday habits [2][5].
Spontaneous Genetic Changes (De Novo Mutations)
In some cases, particularly when craniosynostosis is tied to a broader syndrome, the cause is genetic [6]. However, having a genetic cause does not mean it was passed down through your family. Many of these are de novo mutations—spontaneous genetic changes that happen randomly at the very moment of conception [7].
These spontaneous changes frequently involve specific genes that control bone growth, such as FGFR1, FGFR2, FGFR3, and TWIST1 [6]. A de novo mutation means the genetic alteration was not inherited from you or your partner, and absolutely nothing you did before or during pregnancy triggered it [7][8].
Intrauterine Constraints (Space in the Womb)
Sometimes, the physical mechanics inside the womb play a role in premature suture fusion. This concept is known as intrauterine constraint, which refers to the limited physical space the baby has to grow [9].
Factors that can create physical crowding and apply mechanical pressure to the developing baby’s skull include:
- Carrying multiple babies (twins or triplets)
- An unusual fetal position that places sustained pressure on the head
- Oligohydramnios (having lower than normal levels of amniotic fluid) [9]
Research suggests that these mechanical forces can sometimes contribute to the early closing of a suture [9][4]. Just like genetic variations, intrauterine constraint is a matter of natural biology and physics—it is not caused by your sleeping position, your level of physical activity, or how much you rested while pregnant.
While your medical team will carefully review your full pregnancy history and any medications taken to understand the complete picture [10], it is vital to remember that craniosynostosis is driven by spontaneous genetics and complex fetal development. Letting go of guilt is hard, but understanding these true causes is an important step in focusing your energy on your baby’s care. Keep in mind that with early detection and the guidance of your care team, treatments for craniosynostosis have very high success rates in supporting healthy brain development and reshaping the skull.
Common questions in this guide
Did my diet or stress levels during pregnancy cause my baby's craniosynostosis?
What is non-syndromic craniosynostosis?
How do genetic mutations cause craniosynostosis?
Can limited space in the womb lead to craniosynostosis?
Should my baby undergo genetic testing for craniosynostosis?
Questions to Ask Your Doctor
Curated prompts to bring to your next appointment.
- 1.Was my baby's craniosynostosis classified as isolated (non-syndromic) or is there evidence it might be part of a broader genetic syndrome?
- 2.Would you recommend we see a geneticist or undergo genetic testing, such as a gene panel, to check for spontaneous genetic changes?
- 3.Looking at my pregnancy history and the baby's position in the womb, do you see any signs of intrauterine constraint that might have contributed?
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References
References (10)
- 1
Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.
Ye X, Guilmatre A, Reva B, et al.
Plastic and reconstructive surgery 2016; (137(3)):952-961 doi:10.1097/01.prs.0000479978.75545.ee.
PMID: 26910679 - 2
The Cognitive Profile of Children with Nonsyndromic Craniosynostosis.
Kljajić M, Maltese G, Tarnow P, et al.
Plastic and reconstructive surgery 2019; (143(5)):1037e-1052e doi:10.1097/PRS.0000000000005515.
PMID: 30789480 - 3
Non-syndromic craniosynostosis.
Alperovich M, Tonello C, Mayes LC, Kahle KT
Nature reviews. Disease primers 2025; (11(1)):24 doi:10.1038/s41572-025-00607-4.
PMID: 40210850 - 4
Craniosynostosis: A Reversible Pathology?
Säljö K, Maltese G, Tarnow P, Kölby L
The Journal of craniofacial surgery 2019; (30(6)):1628-1630 doi:10.1097/SCS.0000000000005515.
PMID: 31022145 - 5
Identical Twins Discordant for Metopic Craniosynostosis: Evidence of Epigenetic Influences.
Magge SN, Snyder K, Sajja A, et al.
The Journal of craniofacial surgery 2017; (28(1)):14-16 doi:10.1097/SCS.0000000000003368.
PMID: 28060197 - 6
Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis.
Ibarra-Arce A, Almaraz-Salinas M, Martínez-Rosas V, et al.
Molecular genetics & genomic medicine 2020; (8(8)):e1266 doi:10.1002/mgg3.1266.
PMID: 32510873 - 7
Syndromic Craniosynostosis: A Comprehensive Review.
Katouni K, Nikolaou A, Mariolis T, et al.
Cureus 2023; (15(12)):e50448 doi:10.7759/cureus.50448.
PMID: 38222144 - 8
Genetic Syndromes Associated with Craniosynostosis.
Ko JM
Journal of Korean Neurosurgical Society 2016; (59(3)):187-91 doi:10.3340/jkns.2016.59.3.187.
PMID: 27226847 - 9
Characterization of Perinatal Risk Factors and Complications Associated With Nonsyndromic Craniosynostosis.
Sergesketter AR, Elsamadicy AA, Lubkin DT, et al.
The Journal of craniofacial surgery 2019; (30(2)):334-338 doi:10.1097/SCS.0000000000004997.
PMID: 30358747 - 10
Pharmacological exposures may precipitate craniosynostosis through targeted stem cell depletion.
Durham E, Howie RN, Larson N, et al.
Stem cell research 2019; (40()):101528 doi:10.1016/j.scr.2019.101528.
PMID: 31415959
This page provides educational information about the causes of craniosynostosis during pregnancy. Always consult your pediatrician or maternal-fetal medicine specialist for medical advice regarding your baby's specific diagnosis and care plan.
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