Jinat Fatema, Tripti Rani Das, Sabiha Islam, Bidisha Chakma, Shah Noor Sharmin, Dipika Majumder, Iffat Rahman & Tanzina Iveen Chowdhury·Asian Journal of Pediatric Research·2025
Background: Postpartum iron deficiency anemia remains a significant public health concern globally, specifically concerning women in low-and middle-income countries. In South Asia, involving Bangladesh and India, the prevalence is frighteningly extreme due to factors such as poor...
Open access
Research Article10.9734/ajpr/2025/v15i5449
Background: Acute gastroenteritis is one of the primary causes of pediatric morbidity in developing countries (AGE). Appropriate drug therapy and supportive care are essential to reducing the disease's severity and consequences. Objective: To assess the drug utilization patterns...
Open access
Research Article10.9734/ajpr/2025/v15i5450
Dyggve-Melchior-Clausen syndrome (DMC) is a rare autosomal recessive skeletal dysplasia caused by mutations in the DYM gene, characterized by disproportionate short stature, intellectual disability, and specific radiographic anomalies (EI Ghouzzi et al., 2003, Lapierre et al., 20...
Open access
Research Article10.9734/ajpr/2025/v15i5448
Background: Neonatal lupus erythematosus (NLE) is a rare autoimmune condition resulting from the transplacental transfer of maternal autoantibodies, primarily anti-SSA/Ro and anti-SSB/La. The disease can manifest with cutaneous, cardiac, hematologic, and hepatobiliary involvement...
Open access
Research Article10.9734/ajpr/2025/v15i5447
Peripheral ossifying fibroma (POF) is a reactive, non-neoplastic gingival growth, commonly seen in adolescents and young children, occurring most often in girls. The World Health Organisation (WHO) categorises POF as a fibro-osseous lesion characterised by varied amounts of calci...
Open access
Research Article10.9734/ajpr/2025/v15i5446
Nicolás Padilla -Raygoza, Gilberto Flores-Vargas, Jazmín Alejandra-López-Chávez, Luis Alberto García- Baeza, José Juan Torres-Hernandez, Yareth Valeria Rodríguez-Aguilar & Omar López-Guzmán·Asian Journal of Pediatric Research·2025
Aims: To verify if children hospitalized by COVID-19, met the criteria for Multisystem Inflammatory Syndrome. Study Design: Quantitative, retrospective cohort, retrolective. Place and Duration of Study: Sample: All registries from Guanajuato General Hospital of patients with less...
Open access
Research Article10.9734/ajpr/2025/v15i5445
Bardet-Biedl Syndrome (BBS) is a rare multisystem ciliopathy with autosomal recessive inheritance and genetic heterogeneity, characterised by retinal degeneration, post axial polydactyly, renal disease, hypogonadism, central obesity, several dysmorphic features and variable degre...
Open access
Research Article10.9734/ajpr/2025/v15i5444
Background: While many pregnancies progress normally, some result in preterm birth, a stressful and potentially life-threatening condition for both the mother and infant. Mothers of preterm babies often experience heightened psychological and emotional distress, compounded by cha...
Open access
Research Article10.9734/ajpr/2025/v15i5443
A nine year old child with clinical and radiological features leading to Sly disease, The diagnostic was confirmed with high urinary glycosaminoglycans and very low leukocyte β-glucuronidase activity. This is the first case of MPS VII reported from Morocco.
Open access
Research Article10.9734/ajpr/2025/v15i4442
Background: Pediatric renal failure presents a critical healthcare challenge, necessitating effective renal replacement therapies. Continuous Ambulatory Peritoneal Dialysis (CAPD) has emerged as a preferred modality, particularly in children, due to its feasibility for home-based...
Open access
Research Article10.9734/ajpr/2025/v15i4441
Aims: to reveal the relationship between Gender, Birth Length and Low Birth Weight with Stunting in Kebon Kalapa Village Sumedang in 2021. Methods: using simple cross sectional approach, all primary data obtained from children age between 2-5 years old in Kebon Kalapa Village, Su...
Open access
Research Article10.9734/ajpr/2025/v15i4439
Aim: To highlight a rare presentation of homocystinuria in a pediatric patient, initially manifesting as venous thrombosis, and later diagnosed through multidisciplinary evaluation of systemic features. Case Presentation: A 10-year-old boy, born to third-degree consanguineous par...
Open access
Research Article10.9734/ajpr/2025/v15i4440
AIMS: The aim of this case is to highlight the clinical presentation, diagnostic challenges and treatment outcomes of adrenocortical carcinoma (ACC) in a paediatric patient. It aims to emphasize the importance of early recognition of ACC in children, particularly with signs such...
Open access
Research Article10.9734/ajpr/2025/v15i4438
Background: Mumps is a common viral infection affecting children, primarily involving the salivary glands. However, it can also lead to serious complications, including sensorineural hearing loss. While mumps-related deafness is typically unilateral and sudden in onset, bilateral...
Open access
Research Article10.9734/ajpr/2025/v15i4437
Aim: The aim of this case report was to understand the pleomorphic nature of this rare syndrome and to create awareness regarding the need for multidisciplinary approach towards this disease. Presentation of Case: We report a case of a 5 year 9 month old child, who presented with...
Open access
Research Article10.9734/ajpr/2025/v15i4436