Cleft & Craniofacial Surgery: A Complete Guide for Parents and Patients
Medically reviewed by Dr. Sergio Calleja, DDS, MPH — Board-Certified Oral & Maxillofacial Surgeon · Last reviewed 2026-07-08
If you have just learned that your baby has a cleft lip or cleft palate — whether from a prenatal ultrasound or in the delivery room — take a breath. Clefts are among the most common differences a baby can be born with, and they are also among the most treatable. Between 6,000 and 8,000 children are born with a cleft lip and/or palate in the United States every year — roughly 7,000 children, or about 1 in 600 births. According to updated data published by the National Birth Defects Prevention Network (NBDPN) in 2023, compiled from state health department reports for 2016–2020, about 1 in 1,050 babies is born with a cleft lip with or without a cleft palate, and about 1 in 1,600 babies is born with a cleft palate alone. You are not alone, and neither is your child.
This guide explains, in plain language, what clefts are, how modern team-based care works, and what the surgical journey looks like from the first repair in infancy through the finishing touches in the teenage years. Dr. Calleja is fellowship-trained in cleft and craniomaxillofacial surgery — it is his signature specialty — and he and his team walk families through every stage, in English or Spanish.
What Are Cleft Lip and Cleft Palate?
Early in pregnancy, the tissues that form a baby's face grow toward each other from each side and fuse in the middle — the lip closes between about weeks 4 and 7, and the palate (the roof of the mouth) between about weeks 6 and 10. When that fusion does not fully complete, a gap remains: a cleft lip, a cleft palate, or both. This happens long before most parents even know they are pregnant, and it is not caused by anything a parent did or failed to do. A note on language: while you may see the medical term "birth defect" in older materials, the preferred language for persons born with cleft and craniofacial conditions is "birth difference" — a cleft is one feature of your child, never a definition of them, and that is the language we use in our practice.
Treatment is not one operation — it is a staged journey timed to your child's growth. The lip is typically repaired at around 3 to 6 months of age, the palate at around 9 to 18 months, a small bone graft fills the gap in the gum line at around 7 to 9 years, and — for some patients — jaw surgery and nose refinement complete the picture once growth is finished in the late teens. Each stage is scheduled to protect a specific developmental milestone: feeding, speech, tooth development, and facial balance.
No single doctor can cover all of that alone, which is why the standard of care — set by the American Cleft Palate-Craniofacial Association (ACPA) — is an interdisciplinary cleft team: the surgeon working alongside speech-language pathologists, ear-nose-and-throat (ENT) specialists, orthodontists, audiologists (hearing specialists), pediatric dentists, geneticists, and feeding nurses. Dr. Calleja coordinates this team care so your family has one surgical home from infancy to young adulthood rather than a series of disconnected appointments.
Who We Treat
Cleft and craniofacial care spans every age. Dr. Calleja evaluates and treats:
- Newborns and infants with cleft lip, cleft palate, or both — including prenatal consultations before your baby arrives
- Children who need an alveolar bone graft — the gum-line bone graft typically done around ages 7 to 9, when the adult canine tooth is developing
- Children with speech concerns after palate repair who may need a secondary speech operation
- Teens and young adults with cleft-related jaw differences who need orthognathic (corrective jaw) surgery at skeletal maturity
- Teens and adults seeking revision of the lip or nose as a final refinement
- Adults whose cleft was never fully treated — or was repaired decades ago and deserves modern revision. It is never too late.
What Treatment Achieves
- Comfortable, effective feeding — the first and most immediate goal in infancy
- Clear speech — the palate repair is timed specifically to happen before speech develops
- Better hearing and fewer ear infections, coordinated with ENT care
- Healthy tooth development, with bone grafting that lets adult teeth erupt into a solid gum line
- A natural-looking lip and nose, refined in stages as your child grows
- Confidence — for your child, and for you as parents watching them thrive
- One coordinated surgical home for the entire journey, rather than starting over with a new provider at each stage
Terms You'll Hear
Doctors and patients often use different words for the same thing. Here's how they connect:
- "birth defect (older term)" = birth difference (preferred term)
- The preferred language for persons born with cleft and craniofacial conditions is "birth difference" — it describes the condition without defining the person by it. You will still see "birth defect" in older medical materials and statistics reporting.
- "cleft lip repair" = cheiloplasty
- The operation that closes the gap in the lip and rebuilds the lip muscle — typically done at around 3 to 6 months of age.
- "cleft palate repair" = palatoplasty
- The operation that closes the roof of the mouth and repositions its muscles for speech — typically done at around 9 to 18 months.
- "hole in the palate after surgery" = fistula
- A small opening that can occasionally re-form in the repaired palate; many are harmless, and those that leak food or air can be repaired.
- "gum-line bone graft" = alveolar bone grafting
- A small graft that fills the bony gap in the upper gum line so the adult teeth — especially the canine — can erupt into solid bone.
- "nasal-sounding speech" = velopharyngeal insufficiency (VPI)
- When the repaired palate cannot fully seal off the nose during speech, letting air escape; treated with speech therapy and, if needed, a further operation.
- "upper jaw" = maxilla
- The bone that holds the upper teeth and forms the midface — in some cleft patients it grows underprojected and is repositioned with jaw surgery in the teen years.
- "team care" = interdisciplinary cleft team
- The ACPA standard of care: surgeon, speech pathologist, ENT, orthodontist, audiologist, and other specialists coordinating your child's care together.
- "nose reshaping" = rhinoplasty
- Refinement of the nose — often the final operation of the cleft journey, since a cleft that involves the lip usually affects the shape of the nostril too.
Frequently Asked Questions
What causes cleft lip and palate?
In most cases, a combination of genetics and environment — and often no single identifiable cause at all. Family history plays a role, and factors during pregnancy such as smoking, certain medications, and diabetes have been linked to a somewhat higher chance. But the most important thing for parents to hear is this: a cleft is not your fault. The tissues simply did not finish fusing in the first weeks of pregnancy, usually before anyone knew the pregnancy existed. A genetics consultation — part of standard cleft team care — can tell you whether the cleft is isolated or part of a broader condition.
How many surgeries will my child need in total?
There is no single number, and any surgeon who promises one is guessing. A child with a cleft lip alone may need just one or two operations. A child with a complete cleft lip and palate typically has the lip repair, the palate repair, and an alveolar bone graft — three core operations — and some children also need a speech procedure, jaw surgery in the teen years, or a lip and nose refinement. At each stage, the team recommends surgery only when it protects a real milestone, never by default.
Will my child speak normally?
Most children do. The palate repair is deliberately timed before speech develops — usually by 18 months — so the muscles of the palate can power normal speech sounds from the start. The clear majority of children develop understandable, age-appropriate speech with the help of speech therapy along the way. Published reviews show that roughly one in five children needs an additional operation later to improve speech (for a condition called velopharyngeal insufficiency, or VPI) — and when it is needed, it works well. Your child's speech is monitored by the team at every visit, so nothing is left to chance.
Will there be a scar after cleft lip surgery?
Yes — honesty matters here. Any incision on the skin leaves a scar, and cleft lip repair is no exception. The good news: the repair is designed so the scar sits within the natural lines of the lip, it fades substantially over the first one to two years, and small revisions later in childhood or adolescence can soften it further. Most repaired clefts are far less noticeable than parents fear, and many are hard to spot in everyday life.
Does insurance cover cleft lip and palate surgery?
In nearly all cases, yes. Cleft repair is reconstructive treatment of a congenital (present-at-birth) condition, not cosmetic surgery, and it is typically covered by medical insurance — many states also mandate coverage for cleft-related care. Pre-authorization is standard, and our team handles that paperwork with you, in English or Spanish.
What training does Dr. Calleja have in cleft surgery?
Dr. Calleja is a board-certified oral and maxillofacial surgeon (American Board of Oral and Maxillofacial Surgery) who then completed a dedicated fellowship in Cleft & Craniomaxillofacial Surgery at Charleston Area Medical Center Children's Hospital — an additional year of training focused entirely on cleft and craniofacial care. This is his signature specialty. He has also repaired clefts on surgical mission trips in Kenya and Guatemala, caring for children who would otherwise never receive treatment.
Can adults with an untreated or partially treated cleft still get care?
Absolutely — and this is more common than people realize. Adults who never completed their cleft journey, or whose repairs were done decades ago with older techniques, can benefit from modern bone grafting, jaw surgery, fistula repair, speech surgery, and lip or nose revision. Age is not a barrier; Dr. Calleja evaluates adult cleft patients regularly.
Where does treatment happen, and do you see Spanish-speaking families?
Consultations and follow-up care take place at the Waldorf and California, Maryland offices; the operations themselves are performed in a hospital setting with pediatric anesthesia teams. Dr. Calleja is fully bilingual — Spanish-speaking families hear every explanation, ask every question, and read every instruction in their own language, without an interpreter in the middle.
Have Questions About Cleft & Craniofacial Surgery?
Dr. Calleja evaluates every case personally at the Waldorf and California, MD offices — consultations in English or Spanish.
Related Services
This page is general patient education, not personal medical advice. Every patient's anatomy and health history are different — treatment details, risks, and recovery vary case by case and are reviewed with you during your consultation. For emergencies, call 911.