# Congenital heart disease in neonates with external congenital anomalies in Jos, Nigeria

**Authors:** OO IGE, CS YILGWAN, AS SAGAY, P KANKI, F BODE-THOMAS

PMC · DOI: 10.4103/jomt.jomt_22_19 · Journal of medicine in the tropics · 2026-01-24

## TL;DR

This study found that 30.6% of neonates with external birth defects in Nigeria also had heart defects, highlighting the need for better screening.

## Contribution

The study reports the prevalence of CHD in neonates with external anomalies in a Nigerian setting.

## Key findings

- External congenital anomalies were found in 20.9 per 1,000 neonates.
- 30.6% of neonates with external anomalies also had congenital heart disease.
- Parents of affected neonates had a significantly higher mean age.

## Abstract

Congenital heart disease (CHD) has been found to be more common in neonates with other congenital anomalies and may worsen prognosis. Early diagnosis and treatment of internal congenital anomalies including CHD will improve outcome and decrease neonatal mortality. This study determined the prevalence of CHD among neonates seen with external congenital anomalies in Jos, Nigeria.

We performed complete physical examinations on 2,340 neonates delivered in two tertiary hospitals in Jos, Nigeria. We identified neonates with external congenital anomalies and determined the prevalence of congenital heart defects in them using echocardiography. Data were analysed using STATA 14.0.

External congenital anomalies were present in 49 of the 2,340 neonates recruited − prevalence of 20.9 per 1,000, with a male to female ratio of 1.1:1. Fourteen (28.6%) neonates were syndromic. CHD was present in 15 of 49 (30.6%) neonates studied– prevalence 30.6 per 100. The mean age of the parents with neonates who had external congenital anomalies and CHD was significantly higher than those without CHD.

CHD frequently co-exists with external congenital anomalies especially in syndromic neonates. Hospital-based surveillance systems are needed to capture accurately both internal and external congenital anomalies to improve outcome in these group of neonates.

## Linked entities

- **Diseases:** Congenital heart disease (MONDO:0005453)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** HOCM (MESH:D002312), ASD (MESH:D001321), Folic acid deficiency (MESH:D005494), Prune Belly (MESH:D011535), syndromic (MESH:D013577), Turner's syndrome (MESH:D014424), miscarriage (MESH:D000022), hypertension (MESH:D006973), Congenital (MESH:D008209), external CA (MESH:D017577), cleft lip and palate (MESH:D002971), a ventricular septal defect (MESH:D006345), left ventricular (LV) systolic dysfunction (MESH:D018487), Polydactyly (MESH:D017689), malformation (MESH:C564254), anomaly in the musculoskeletal system (MESH:D009139), VSD (MESH:D004310), Down syndrome (MESH:D004314), anterior abdominal (MESH:D000007), developmental anomaly (MESH:C566440), deaths (MESH:D003643), dysmorphic (MESH:D057215), CNS (MESH:D002494), neonatal sepsis (MESH:D000071074), Sacrococcygeal tumour (MESH:D009369), atrial (MESH:D064752), anorectal malformation (MESH:D000071056), infectious diseases (MESH:D003141), chromosomal abnormality (MESH:D002869), Trisomy 18 (MESH:D000073842), 5Congenital anomalies (MESH:D000013), bicuspid aortic valve (MESH:D000082882), skeletal anomalies (MESH:C535534), Tetralogy of Fallot (MESH:D013771), spina bifida (MESH:D016135), Baraister-Winter syndrome (MESH:D016574), External congenital anomalies (MESH:C580012), AVSD (MESH:C562831), gastrointestinal (GIT) anomalies (MESH:D005767), cor-triatriatum dexter (MESH:D003310), dextrocardia (MESH:D003914), Isolated malformations (MESH:C565377), -Weidemann (MESH:C565755), CHD (MESH:D006330), HIV (MESH:D015658), DM (MESH:D003920), PAPVR (MESH:D012587)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12830049/full.md

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Source: https://tomesphere.com/paper/PMC12830049