What Is the Risk of a Second Baby with Cleft Lip or Palate?
At a Glance
After one baby has a cleft lip or palate that occurs by itself, the chance in one future pregnancy is generally about 2% to 5%, but the personal estimate may differ based on the cleft type, family history, and whether a genetic syndrome is identified.
In this answer
4 sections
If your first baby was born with a cleft lip or palate, it is completely normal to worry about the chances of it happening again in a future pregnancy. Please know that for most families, an isolated cleft is not caused by anything the parents did or didn’t do [1]. For the majority of families where the first baby has an isolated cleft (meaning there are no other known health issues or syndromes), the empiric recurrence risk for one future pregnancy is generally estimated to be around 2% to 5% [1]. However, this rough population estimate is not a cumulative lifetime percentage, and your personal risk can change depending on your family history, the exact type of cleft, and whether a specific genetic syndrome is identified [2][3].
Isolated vs. Syndromic Clefts
To understand your specific risk, doctors look closely at whether the cleft is “isolated” or “syndromic” [2].
- Isolated (Non-syndromic) Clefts: “Isolated” means that the cleft is the only recognized medical anomaly the baby has. It does not mean there are no genetic factors involved; rather, isolated clefts are usually caused by a complex, overlapping mix of many genetic and environmental factors [1][4]. If your child has an isolated cleft, the chance of recurrence in a future pregnancy is typically lower, around the 2-5% general estimate [1].
- Syndromic Clefts: Sometimes a cleft is just one feature of a larger genetic syndrome, meaning the child’s overall examination might also show heart, kidney, or developmental differences [5]. Keep in mind that many children with clefts do not have a syndrome. But if a specific genetic syndrome is identified, the risk of having another child with a cleft is determined by that condition and can be significantly higher [6].
Types of Clefts Matter
The medical community considers a cleft lip (with or without a cleft palate) and a cleft palate only to be distinct conditions [7]. Rather than having entirely different causes, they have partly different patterns of genetic and environmental risk [8]. The exact type of cleft your child has, as well as the child’s sex, are factors used in population estimates [9]. Because of this complexity, specialists may use specialized tools that factor in your ancestry, the child’s sex, the type of cleft, and your detailed family history to estimate your personalized recurrence risk [10].
The Importance of Genetic Counseling
Even if you are not yet ready to conceive, it is highly recommended to meet with a clinical geneticist or a genetic counselor [3]. A specialist will:
- Review your child’s records: They will look at medical diagnoses, physical exams, and any genetic testing [5]. Note that routine genetic testing isn’t automatically needed for every isolated cleft; it is more strongly considered if there are other physical features, developmental concerns, or a strong family history. Furthermore, a negative genetic test does not eliminate the risk of recurrence.
- Map your family history: They will look at a three-generation family history from both parents, as having multiple affected relatives can increase your risk estimate [11][12].
- Discuss medications and supplements: They will review any medications or supplements you take. You should never stop prescribed medicines without medical advice. They will also discuss following evidence-based guidelines for preconception folic acid, though it is important to know that folic acid does not guarantee prevention of all clefts [1].
Planning for a Future Pregnancy
If you decide to have another child, your care team can discuss options for prenatal screening. A detailed fetal anatomy ultrasound (commonly done around 18–22 weeks) can often detect a cleft lip. However, an isolated cleft palate can be very difficult or impossible to see before birth, so a normal ultrasound cannot completely rule out a cleft. Your team may also discuss diagnostic tests like amniocentesis or chorionic villus sampling (CVS), which assess chromosomal or genetic conditions but do not directly diagnose a cleft; these tests are not automatically required for every pregnancy.
Common questions in this guide
If my first baby had an isolated cleft, what is the chance it will happen again?
Does having a cleft mean my child has a genetic syndrome?
Can genetic counseling give me a more personal recurrence-risk estimate?
Should my child or I have genetic testing before another pregnancy?
Can an ultrasound find a cleft during a future pregnancy?
Can folic acid prevent a second cleft?
Do amniocentesis or CVS diagnose cleft lip or palate?
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Questions to Ask Your Doctor
Curated prompts to bring to your next appointment.
- 1.Was our child's cleft determined to be isolated, or should we be evaluated for a potential underlying genetic syndrome?
- 2.Based on our specific family history and our child's exact type of cleft, what is our personalized recurrence risk for a future pregnancy?
- 3.Would genetic testing be helpful for our child or for us as parents to clarify our recurrence risk?
- 4.What can a detailed fetal anatomy ultrasound detect in a future pregnancy, and what could it potentially miss?
- 5.Would you recommend a referral to a maternal-fetal medicine specialist for our next pregnancy?
References
References (12)
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Genes 2023; (14(8)) doi:10.3390/genes14081603.
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The impact of developmental genes in non-syndromic cleft lip and/or palate
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Journal of the Turkish German Gynecological Association 2023; (24(1)):57-64 doi:10.4274/jtgga.galenos.2022.2021-10-7.
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PMID: 31538461 - 5
A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate.
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PMID: 28515470 - 6
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Human mutation 2015; (36(11)):1029-33 doi:10.1002/humu.22827.
PMID: 26123647 - 7
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.
Leslie EJ, Carlson JC, Shaffer JR, et al.
Human genetics 2017; (136(3)):275-286 doi:10.1007/s00439-016-1754-7.
PMID: 28054174 - 8
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Alade A, Peter T, Busch T, et al.
Genetic epidemiology 2024; (48(6)):258-269 doi:10.1002/gepi.22564.
PMID: 38634654 - 9
Birth prevalence of cleft lip and/or palate - a register study of all children born in Sweden years 2000-2020.
Cornefjord M, Källén K, Klintö K, et al.
Journal of plastic surgery and hand surgery 2025; (60()):120-126 doi:10.2340/jphs.v60.43739.
PMID: 40457887 - 10
CLEFT RR- New app to Calculate Recurrence Risk in Cleft lip and Palate.
Lacerda RHW, Mendonça ACG, Laurentino RA, et al.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2024; (61(12)):2097-2102 doi:10.1177/10556656231191346.
PMID: 37545187 - 11
Family History of Nonsyndromic Orofacial Clefts: A Brazilian Multicenter Study.
de Barros LP, Machado RA, das Neves LT, et al.
Oral diseases 2025; (31(7)):2243-2250 doi:10.1111/odi.15273.
PMID: 39888182 - 12
Prevalence of orofacial clefts and risks for nonsyndromic cleft lip with or without cleft palate in newborns at a university hospital from West Mexico.
Corona-Rivera JR, Bobadilla-Morales L, Corona-Rivera A, et al.
Congenital anomalies 2018; (58(4)):117-123 doi:10.1111/cga.12276.
PMID: 29457660
This page provides general information about recurrence risk for cleft lip or palate and is not medical advice. A genetic counselor or other qualified clinician can assess your family's individual risk.