# Patterns and Associated Factors of Congenital Anomalies Among Neonates in 14 Yemeni Governorates 2021–2023: A Case: Control Study

**Authors:** Hiam Al-Atnah, Anas Al-Qubati, Amir Addin Al-Hashedi, Muath Al-Saidy, Saleh Al-Shawish, Moamer M. Badi, Najeeb Al-Qubati, Yasser Ghaleb, Maha Al-Muntaser

PMC · DOI: 10.1016/j.gloepi.2025.100196 · Global Epidemiology · 2025-03-14

## TL;DR

This study examines the patterns and risk factors for congenital anomalies in neonates across 14 Yemeni governorates from 2021 to 2023.

## Contribution

The study provides new insights into the regional distribution and risk factors for congenital anomalies in Yemen.

## Key findings

- Al Hudaydah, Ibb, and Sana'a had the highest rates of congenital anomalies.
- Consanguinity and low socioeconomic status were strongly associated with congenital anomalies.
- The nervous system was the most commonly affected system.

## Abstract

Long-term disability and a reduced quality of life are often associated with congenital anomalies (CAs), which present as structural, functional, or metabolic defects. This study provides a comprehensive view of neonatal congenital anomalies in 14 Yemeni governorates, a significant but often overlooked public health concern. The current study aimed to determine the patterns and associated factors of congenital anomalies in 14 Yemeni governorates between 2021 and 2023.

An unmatched case-control 1:2 design was conducted using secondary data collected from various health facilities across 14 Yemeni governorates during 2021–2023. Sample size was calculated and data was analyzed using Epi Info version 7.2, with 612 neonates with documented diagnosis of congenital anomalies and 1224 healthy neonates. Binary and multiple logistic regression were used to identify factors associated with congenital anomalies, alongside the chi-square test.

The majority of the congenital anomalies identified were located in Al Hudaydah (34 %), Ibb (17.2 %), and Sana'a (13.1 %). Most were isolated 518 (84.64 %), whereas 94 (15.36 %) were multiple. The predominant system was the nervous system (33.9 %), followed by the skeletal system (14.8 %) and orofacial anomalies (10.6 %). Furthermore, strong associations were found with positive consanguinity (OR = 28.82), low socioeconomic status (OR = 10.70), maternal age ≥ 35 years old (OR = 7.66), stress (OR = 4.95), acute diseases (OR = 3.56), gestational age < 37 weeks (OR = 3.32), maternal age < 20 years old (OR = 2.32), positive family history (OR = 1.74), low birth weight (OR = 1.27), grand-multiparity (OR = 0.71) and male sex (OR = 0.10).

This broad research identified significant patterns, maternal and neonatal associations, and protective variables for congenital anomalies. These results can help inform national interventions and policies for prevention and improving neonatal care.

This study was self-funded by the authors and did not receive any external funding or any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

## Full-text entities

- **Diseases:** disability (MESH:D009069), , functional, or metabolic defects (MESH:D008661), CAs (MESH:D000013), orofacial anomalies (MESH:D020820)

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC11995116/full.md

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Source: https://tomesphere.com/paper/PMC11995116