Most Common Birth Defects in the US. – Regional Data Breakdown

Illustration comparing a baby with and without a cleft lip, highlighting one of the most common birth defects

When it comes to birth defects in the U.S., there’s no single, nationwide tracking system keeping tabs on every case. Instead, most states maintain their tracking programs, providing us with valuable regional data that helps paint a picture of which birth defects are most common and where.

Across the country, certain defects consistently show up at higher rates, and understanding these patterns is essential for healthcare providers, policymakers, and families.

Let’s start with the facts from the CDC: clubfoot affects roughly 1 in 536 births, which translates to around 6,850 babies born with this condition annually.

Down syndrome (Trisomy 21), one of the most well-known chromosomal conditions, occurs in 1 in 643 births, impacting approximately 5,713 babies each year. While these numbers represent national estimates, variations exist across different regions based on factors like environmental exposures, genetics, and access to prenatal care.

Key Takeaways

  • Clubfoot and Down syndrome are among the most common birth defects, affecting thousands of babies yearly.
  • Neural tube defects, while less common, have significant impacts and highlight the importance of folic acid supplementation.
  • Heart defects represent the largest category, with nearly every state seeing cases annually.
  • Regional variations stem from differences in healthcare access, environmental factors, and public health initiatives.

Heart Defects: The Most Common Category of Birth Defects

Congenital heart defects (CHDs) make up the largest category of birth defects, with some types requiring complex surgeries or lifelong management. Their prevalence and severity can vary widely.

Heart Defect Occurrence Rate Estimated Babies Affected Annually
Atrioventricular septal defect (AVSD) 1 in 1,712 births ~2,145
Coarctation of the aorta 1 in 1,712 births ~2,146
Common truncus (TA) 1 in 15,984 births ~230
Double outlet right ventricle (DORV) 1 in 4,237 births ~867
Ebstein anomaly 1 in 12,916 births ~284
Hypoplastic left heart syndrome (HLHS) 1 in 3,955 births ~929
Interrupted aortic arch (IAA) 1 in 10,058 births ~365
Pulmonary valve atresia and stenosis 1 in 972 births ~3,779
Pulmonary valve atresia 1 in 6,708 births ~548
Single ventricle 1 in 15,356 births ~239
Tetralogy of Fallot (TOF) 1 in 2,077 births ~1,768
Total anomalous pulmonary venous connection (TAPVC) 1 in 7,552 births ~486
Transposition of the great arteries (TGA) 1 in 3,348 births ~1,097
Dextro-transposition of great arteries (d-TGA) 1 in 3,957 births ~928
Tricuspid valve atresia and stenosis 1 in 5,527 births ~665
Tricuspid valve atresia 1 in 11,309 births ~325

These defects account for a significant number of newborn health challenges across the U.S. Pulmonary valve defects, for example, affect nearly 3,800 babies annually. Regions with robust pediatric cardiology services often report higher detection and management rates.

According to CDC data, congenital heart defects like atrioventricular septal defect (1 in 1,712 births) and pulmonary valve atresia and stenosis (1 in 972 births) are among the most frequently reported, affecting thousands of babies each year.

Neural Tube Defects: Serious but Rare Conditions

 

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A 2022 study published in Birth Defects Research highlighted significant regional disparities in neural tube defect rates across the United States, emphasizing the impact of factors such as maternal folic acid intake, healthcare access, and environmental exposures on the prevalence of these conditions.

Neural Tube Defect Occurrence Rate Estimated Babies Affected Annually
Anencephaly 1 in 5,246 births ~700
Encephalocele 1 in 10,365 births ~354
Spina bifida (without anencephaly) 1 in 2,875 births ~1,278

Anencephaly, where parts of the brain and skull don’t form, is typically fatal shortly after birth. Spina bifida, a defect in the spine, varies in severity and can lead to lifelong mobility and health issues.

The rates of these defects can be influenced by factors like maternal folic acid intake, genetics, and access to prenatal care. States with aggressive folic acid supplementation programs have seen reductions in neural tube defects.

Eye Defects: Less Common but Impactful

A young child with a visible eye defect affecting one eye
Source: Youtube/Screenshot, Anophthalmia and microphthalmia affect around 1 in 5,078 births

Defects affecting eye formation, like anophthalmia (absence of one or both eyes) and microphthalmia (abnormally small eyes), occur less frequently but present significant challenges for affected children.

According to CDC data, eye defects like anophthalmia and microphthalmia occur in about 1 in 5,078 births, affecting roughly 723 babies annually across the U.S.

Eye Defect Occurrence Rate Estimated Babies Affected Annually
Anophthalmia/Microphthalmia 1 in 5,078 births ~723

Cleft Lip and Palate: Common and Treatable

An infant with a visible cleft lip being held by a caregiver, showing a common congenital facial condition
Source: Youtube/Screenshot, Cleft lip, with or without palate, affects about 1 in 1,032 births

Mouth and facial defects, particularly cleft lip and cleft palate, are among the most common congenital defects. These conditions are highly treatable with surgical intervention, but early diagnosis and coordinated care are critical.

According to the latest data, cleft lip with or without cleft palate occurs in about 1 in 1,032 births, translating to roughly 3,560 babies born each year with this condition.

Defect Occurrence Rate Estimated Babies Affected Annually
Cleft lip with/without palate 1 in 1,032 births ~3,560
Cleft lip with cleft palate 1 in 1,583 births ~2,320
Cleft lip alone 1 in 2,963 births ~1,240
Cleft palate alone 1 in 1,583 births ~2,321

Regional differences can reflect access to prenatal care, maternal health factors, and public health campaigns promoting awareness of risk factors like smoking during pregnancy.

Muscle and Bone Defects: Clubfoot and Limb Deficiencies

@doctor.bradley #clubfoot The majority of Americans aren’t familiar with clubfoot; it’s a disability where the foot turns inward so severely that the bottom of the foot faces sideways or even upward, which leads to extreme pain, stigma and often an inability to walk. It’s one of the most common birth defects globally and can become a lifelong disability if it’s not treated. We’re fortunate that here in the United States, clubfoot is detected early, often, even in utero and babies born with the condition receive the highest levels of medical treatment. Yet, 85% of children in low- and middle-income countries born with clubfoot do not have access to the care or health practitioners needed to change the trajectory of this diagnosis. @MiracleFeet is an organization on a mission to ensure all children with #clubfoot ♬ original sound – Doctor Brad

Clubfoot is the most common musculoskeletal birth defect, while limb deficiencies affect fewer children but often require specialized care.

Defect Occurrence Rate Estimated Babies Affected Annually
Clubfoot 1 in 536 births ~6,850
Diaphragmatic hernia 1 in 3,214 births ~1,143
Gastroschisis 1 in 2,439 births ~1,506
Limb deficiencies 1 in 2,064 births ~1,779
Omphalocele 1 in 4,021 births ~914

According to NCBI estimates, clubfoot remains the most common musculoskeletal birth defect, affecting about 1 in 536 births, or around 6,850 babies annually.

These cases often require specialized orthopedic care and prosthetics to support mobility and function.

Other musculoskeletal defects include diaphragmatic hernia, occurring in about 1 in 3,214 births (roughly 1,143 babies annually), and gastroschisis, seen in 1 in 2,439 births (affecting about 1,506 babies annually).

Gastroschisis is a condition where the baby’s intestines extend outside of the body through a hole near the belly button, often necessitating surgery soon after birth.

Meanwhile, omphalocele, a related but distinct condition, occurs in 1 in 4,021 births and affects around 914 babies each year, involving a protective sac around the protruding organs. These defects vary in severity and management, but all require coordinated medical care.

Stomach and Intestine Defects: Challenging Conditions

Medical illustration showing the digestive tract inside the ribcage, highlighting congenital stomach and intestinal defects
Source: Youtube/Screenshot, Esophageal and rectal defects show why early detection and prenatal care matter

Gastrointestinal defects like esophageal atresia and rectal atresia can complicate feeding and digestion, often requiring early surgery.

Defect Occurrence Rate Estimated Babies Affected Annually
Esophageal atresia/tracheoesophageal fistula 1 in 4,167 births ~882
Rectal and large intestinal atresia/stenosis 1 in 2,220 births ~1,654

According to national estimates, gastrointestinal defects such as esophageal atresia occur in about 1 in 4,167 births, impacting roughly 882 babies each year.

Esophageal atresia is a condition where the esophagus doesn’t connect properly to the stomach, requiring surgery soon after birth to enable proper feeding. Similarly, rectal and large intestinal atresia or stenosis, affecting approximately 1 in 2,220 births (around 1,654 babies annually), involves a narrowing or complete blockage of the lower digestive tract.

This condition often necessitates early surgical intervention and can lead to long-term bowel management issues.

Both esophageal and rectal defects highlight the importance of prenatal care and early detection, as well as the need for experienced pediatric surgical teams to ensure the best outcomes.

Chromosomal Anomalies: The Genetic Side

Chromosomal conditions, especially Down syndrome (Trisomy 21), are among the most recognized birth defects. These anomalies can affect various body systems and are influenced by maternal age and regional prenatal screening practices.

Condition Occurrence Rate Estimated Babies Affected Annually
Trisomy 13 1 in 6,967 births ~527
Trisomy 18 1 in 3,336 births ~1,101
Trisomy 21 (Down syndrome) 1 in 643 births ~5,713

According to CDC data, Down syndrome (Trisomy 21) stands as the most common chromosomal anomaly in the U.S., occurring in approximately 1 in every 643 births and affecting an estimated 5,713 babies annually.

This condition arises from an extra copy of chromosome 21, leading to a range of physical and developmental challenges that vary widely in severity. The prevalence of Down syndrome is influenced by several factors, including maternal age, with older mothers facing a higher risk.

Advances in prenatal screening and diagnostic testing have made it possible to identify this condition early, offering families time to plan and connect with resources. Despite the challenges, many children with Down syndrome lead fulfilling lives, thanks to early interventions, medical care, and supportive environments.

Regional differences in diagnosis rates may reflect disparities in access to prenatal care and screening services, highlighting the need for consistent healthcare outreach across the country

Birth Defect Prevalence in Selected States

State Musculoskeletal Defects Cardiac Defects Neural Tube Defects Orofacial Clefts Data Source
Texas 165 per 10,000 158 per 10,000 Data not specified Data not specified
Arkansas Data not specified Data not specified Higher than the national average Higher than the national average State Surveillance Reports
Kentucky Data not specified Data not specified Elevated rates Higher prevalence State Surveillance Reports
Alabama Data not specified Increased prevalence Data not specified Data not specified State Surveillance Reports
Mississippi Data not specified Data not specified Data not specified Data not specified

1. Musculoskeletal Defects

  • Texas leads the data with 165 cases per 10,000 live births, indicating a significantly high prevalence of musculoskeletal anomalies, which likely includes conditions like clubfoot and limb deficiencies.
  • Other states did not specify detailed numbers, but higher prevalence may also be present in Arkansas and Kentucky, which are regions known for limited healthcare access in rural areas.

The high prevalence in Texas may reflect both an increased detection rate due to comprehensive surveillance and potentially higher risk factors such as environmental exposures or maternal health issues.

2. Cardiac Defects

  • Texas reports 158 cases per 10,000 live births for cardiac defects, a figure consistent with national trends but indicating a substantial healthcare burden.
  • Alabama shows an increased prevalence, suggesting either higher incidence or improved case detection, though specific rates are not provided.

Congenital heart defects are the most common type of birth defect nationwide. States with strong pediatric cardiology services, like Texas, may report higher prevalence due to better diagnosis and data collection. Environmental factors or maternal health (e.g., diabetes, obesity) may also contribute.

3. Neural Tube Defects

Diagram showing different types of neural tube defects in babies
Source: Youtube/Screenshot, Folic acid programs help reduce neural tube defect rates
  • Arkansas and Kentucky both report higher-than-national-average rates of neural tube defects, including anencephaly and spina bifida.
  • Data for Texas, Alabama, and Mississippi is not specified, though these states may still experience elevated rates in certain regions.

High neural tube defect rates in Arkansas and Kentucky may correlate with inadequate folic acid intake, socioeconomic barriers, or environmental risk factors. Public health initiatives like folic acid supplementation have been shown to lower these rates.

4. Orofacial Clefts (Cleft Lip and/or Palate)

  • Arkansas and Kentucky report higher prevalence of orofacial clefts than the national average, while Texas, Alabama, and Mississippi lack specified data.
  • These defects are influenced by both genetic and environmental factors, including maternal smoking, diabetes, and certain medications.

Higher rates in Arkansas and Kentucky suggest possible gaps in maternal health services, nutrition education, or smoking cessation programs.

Methodology

To write this article, we first compiled and reviewed data from multiple sources, including the CDC, National Birth Defects Prevention Network, and state-level surveillance reports. We prioritized clarity and accuracy, focusing on prevalence rates and the number of babies affected each year.

From there, we structured the content to balance detailed data with context, offering readers not just numbers but also explanations of underlying causes, risk factors, and implications.

Where possible, we highlighted regional differences to give a fuller picture of how birth defect rates vary across the U.S. We also integrated recent studies, like the 2022 paper in Birth Defects Research, to ensure the information was grounded in current science.

Finally, we aimed for an engaging, approachable tone that informs readers while respecting the seriousness of the subject.

The Takeaway: Why Awareness and Early Action Matter

Birth defects affect thousands of babies across the U.S. every year, with clubfoot and Down syndrome among the most common.

While rates vary by region, the overall message is clear: early detection, access to high-quality prenatal care, and public health education are essential to reducing risks and improving outcomes.

Knowing which defects are more prevalent in certain areas helps healthcare providers and policymakers focus resources where they’re needed most.

For families, understanding these patterns can offer reassurance and guide proactive steps, from genetic counseling to connecting with local support programs. Staying informed—and advocating for strong tracking and early intervention systems—can make a real difference.

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