Copyright
©The Author(s) 2025.
World J Clin Pediatr. Sep 9, 2025; 14(3): 106439
Published online Sep 9, 2025. doi: 10.5409/wjcp.v14.i3.106439
Published online Sep 9, 2025. doi: 10.5409/wjcp.v14.i3.106439
Table 1 Laboratory findings
Parameter | Findings |
Blood group | A+ |
White blood cell count | 10000 × 109/L |
Haemoglobin | 14.9 g/dL |
Platelets | 253000 |
C-reactive protein | Non-reactive |
Blood cultures | Negative |
Table 2 Summary of reported cases of truncus arteriosus with scoliosis or related syndromes
Ref. | Patient demographics | Associated anomalies | Truncus arteriosus type | Management | Outcome |
Alizadeh et al[7], 2022 | Newborn, unspecified | Hypoplastic left heart syndrome, other cardiovascular defects | Type II | Multidisciplinary management, palliative care | Not specified |
Takeuchi et al[8], 2018 | Infant, unspecified | Interrupted aortic arch, bronchial compression | Unspecified | Pulmonary artery stenting, surgery | Post-op bronchial issues |
Abdelaal et al[9], 2022 | Neonate, unspecified | Coarctation of the aorta, truncal valve regurg | Common arterial trunk | Surgery | Survived post-surgery |
Chen et al[10], 2016 | Infants to adults | Truncal valve anomalies, other cardiac issues | Mixed (I, II, III) | Surgical repair across age spectrum | Variable, mostly positive |
Present study, 2025 | Preterm neonate, female | None confirmed, limited resources for genetic testing | Type I | Supportive care | Awaiting surgical correction |
- Citation: Omullo P, Nurani KM, Shahabi K, Emma O, Mutuku B. Congenital scoliosis with truncus arteriosus type 1 in a preterm neonate: A case report. World J Clin Pediatr 2025; 14(3): 106439
- URL: https://www.wjgnet.com/2219-2808/full/v14/i3/106439.htm
- DOI: https://dx.doi.org/10.5409/wjcp.v14.i3.106439