Skip to content

All published articles 575

Early Initiation of Breastfeeding and Associated Factors in a Private Healthcare Facility in Port Harcourt, Nigeria: A Before-and-After PDSA Cycle Study

Ozigbo Chinelo, Juliana & Okorie Elizabeth-Martha · Asian Journal of Pediatric Research · 2026

Background: Early breastfeeding initiation ensures that the newborn receives the nutrients- and immunoglobulin-rich colostrum, reduces reliance on prelacteal feeds and promotes exclusive breastfeeding, protecting the child from infections and offering other health benefits that s...

Open access Research Article 10.9734/ajpr/2026/v16i5543

Rare Genetic Ataxias in Childhood and Future Implications for Curing Gene Therapy Options

Stefan Bittmann, Elisabeth Luchter & Elena Moschüring-Alieva · Asian Journal of Pediatric Research · 2026

Rare genetic ataxias in childhood are usually progressive neurological disorders characterized by coordination problems (balance/gait instability, fine motor skills) due to damage to the cerebellum. Ataxias are movement disorders that mainly originate from the cerebellum and its...

Open access Research Article 10.9734/ajpr/2026/v16i5542

A Rare Case of Anti-metabotropic Glutamate Receptor 1 (mGluR1) Antibody-Associated Autoimmune Encephalitis in a School Going Age Child Related to Nursing Experience

Peng Meiyue, Sun Wanjun, Zhang Xipin, Jiao Fuyong & Zheng Qianqian · Asian Journal of Pediatric Research · 2026

Background: Autoimmune encephalitis (AE) encompasses a group of central nervous system inflammatory disorders mediated by autoimmune mechanisms, characterized by diverse clinical manifestations including psychiatric abnormalities, cognitive impairment, and motor deficits. Anti-me...

Open access Research Article 10.9734/ajpr/2026/v16i4541

Tuberculous Meningitis in a Young Adolescent: A Diagnostic Conundrum

Lere P. Oluwadare, Pauline K. Akowundu, Joshua O. Awofeso, Oladotun V. Olalusi, Oyindamola O. Aderinto, Adebowale T. Odunafolabi, Sampson C. Aliozor, Christian E. Amiwero, Olatunbosun O. Olawanle & Odutola I. Odetunde · Asian Journal of Pediatric Research · 2026

The occurrence of tuberculous meningitis in children is relatively rare, but it is associated with higher rates of mortality and severe morbidity. Confirmation of diagnosis is often difficult, and other infectious aetiologies such as bacterial, viral and fungal causes must be rul...

Open access Research Article 10.9734/ajpr/2026/v16i4540

Rare Short Stature Disorders in Childhood: Future Implications for Treatment and Gene Therapy Options

Stefan Bittmann, Elisabeth Luchter & Elena Moschüring-Alieva · Asian Journal of Pediatric Research · 2026

Rare childhood short stature disorders such as Achondroplasia, Hypochondroplasia, ACAN syndrome, and Noonan Syndrome are primarily caused by specific genetic mutations that disrupt normal bone growth and development. Advances in molecular diagnostics have improved early detection...

Open access Research Article 10.9734/ajpr/2026/v16i4539

Delayed Reimplantation of an Avulsed Maxillary Central Incisor Following Extended Extra-oral Dry Time: A Case Report

Dipali Vetal, Jyothsna V. Setty, Maheshkumar Karuppiah, Utkarsh Patil, Anushka Choche & Arunkumar S · Asian Journal of Pediatric Research · 2026

Background: Tooth avulsion is the complete displacement of a tooth from its alveolar socket, causing damage to the periodontal structures. Although relatively uncommon, it represents 1–16% of traumatic dental injuries and is most frequently seen in the maxillary anterior region....

Open access Research Article 10.9734/ajpr/2026/v16i4538

Management of Traumatic Injuries in Visually Impaired Child with Modified Behaviour Management Techniques: A Case Report

Dipali Vetal, Jyothsna V Setty, Mahesh Kumar Karuppiah, Anushka Choche, Atharv Kulkarni & Utkarsh Patil · Asian Journal of Pediatric Research · 2026

The prevalence of childhood blindness varies worldwide, affecting approximately 0.3 per 1,000 children in industrialized nations, 1.2 per 1,000 in developing countries, and up to 1.7 per 1,000 in India. Visual impairment significantly impacts a child's ability to navigate their e...

Open access Research Article 10.9734/ajpr/2026/v16i4537

Awareness of Caregivers Regarding Pediatric Medications administration and preparation to Children Attending Mohamed Alamin Hamid Pediatrics Hospital, Sudan

Wafa Babiker Elamin Abdulmalik, Widad Alsheikh Mustafa, Abdelwaged Abdelrhman Omer, Hamed Elneel Maryoud & Khalid Yousif Ahmed Algaali · Asian Journal of Pediatric Research · 2026

Introduction: Ensuring proper children drug utilization is essential for successful treatment.  Several studies have reported various problems including dosing errors and drug misuse, including use without prescription. There is a lack of data regarding this issue in Sudan where...

Open access Research Article 10.9734/ajpr/2026/v16i3534

From the Hierarchy of Abilities and Skills (HAS) to an Integrated Pediatric and Educational Therapies (IPET) Framework: A Conceptual Model for Assessment and Intervention

Kok Hwee Chia, Meng Kiat Tan & Xuelian Jia · Asian Journal of Pediatric Research · 2026

To understand child development, the Hierarchy of Abilities & Skills (HAS) model provides a structured framework through sequential levels of functioning that range from biological foundations to higher-order cognitive and metacognitive processes. The authors aim to extend th...

Open access Research Article 10.9734/ajpr/2026/v16i3535

Serum Sodium and Inflammatory Hematologic Indices as Predictors of Febrile Seizure Subtypes among Children in Southern Coastal Region Government Medical College Hospital, India

M. Santhana Kumar, M. Selvamuthu, C. Gowcigan, G. Karthikeyan, V.V. Sathyaseelan & V. Srinivasan · Asian Journal of Pediatric Research · 2026

Background: Febrile seizures (FS) are the most common neurological disorder in children and continue to cause worry for parents and caregivers. Clinical and lab assessments are important for identifying risk factors and guiding treatment. Objective: To evaluate the demographic, c...

Open access Research Article 10.9734/ajpr/2026/v16i3533

Cerebral Intraparenchymal Hemorrhage Presenting as Global Myocardial Hypokinesia in Term Newborn: A Case Report

Kiran Kumar Haridas, D. Kalashankar, K. Vaishnavi, T. Naveen & P. Ramesh · Asian Journal of Pediatric Research · 2026

Background: Intracranial hemorrhage (ICH) in neonate has devastating morbidity and long term sequel. The most common presentation of ICH is seizures. We present a rare case of ICH presenting as severe myocardial dysfunction termed as neurogenic stunned myocardium (NSM) in a neona...

Open access Research Article 10.9734/ajpr/2026/v16i3532

Isolated Bilateral Pleural Effusion in Acute Hepatitis A Infection: A Rare Pediatric Presentation

Rishabh Dubey, Mustafa Khan & Ajay Punj · Asian Journal of Pediatric Research · 2026

Background: Hepatitis A virus (HAV) infection remains a significant cause of acute viral hepatitis among children in developing regions. Although the illness is predominantly self-limiting and primarily affects the liver, atypical systemic manifestations have occasionally been re...

Open access Research Article 10.9734/ajpr/2026/v16i3531

The Clinical and Hemodynamic Influence on Ductal Closure to Acetaminophen Therapy in High-risk Extreme Low Gestational Age Newborns

Joyce Khoo May Lyn, Ooi Boon Siew, Lin Jiaying, Abdul Alim Abdul Haium, Gloria Lee Chun Yan, Tan Min Yu, Victor Samuel Rajadurai & Krishna Revanna Gopagondanahalli · Asian Journal of Pediatric Research · 2026

Aim: To compare clinical and echocardiographic characteristics between infants with successful ductal closure and persistent PDA post-acetaminophen treatment. Design: Single center clinical audit. Patients: Infants born< 28 weeks gestation. Place and Duration of Study: Tertiar...

Open access Research Article 10.9734/ajpr/2026/v16i3530

Geroderma Osteodysplasticum Associated with Severe Factor V Deficiency in a Pediatric Patient: A Case Report

R. Acharafi, S. Sabbar, A. Baaziz & A. MDAGHRI ALAOUI · Asian Journal of Pediatric Research · 2026

Background: Geroderma osteodysplasticum (GO) is a rare autosomal recessive connective tissue disorder caused by variants in GORAB (golgin, RAB6 interacting), located on chromosome 1q24.2. The phenotype may mimic Ehlers–Danlos syndrome (EDS) or hereditary cutis laxa. Case Presenta...

Open access Research Article 10.9734/ajpr/2026/v16i3529