Introduction: Marden Walker Syndrome is a rare genetic disorder with distinctive craniofacial features, primarily characterized by micrognathia or a small jaw. Patients' affected by this condition may undergo corrective surgical procedures in order to manage their deformities and...
Open access
Research Article10.9734/ajpr/2024/v14i12410
Background: Undescended testis (UDT), or cryptorchidism, is a prevalent pediatric condition with significant implications for fertility and malignancy risk if untreated. Affecting 1–5% of male infants, UDT is influenced by genetic, hormonal, and environmental factors. Methods: T...
Open access
Research Article10.9734/ajpr/2024/v14i12409
Various cargo vesicles containing presynaptic proteins are transported from the neuronal cell body to the neuronal terminal to aid in active zone formation. Researchers showed altered levels up to 25 different synaptic proteins (SNAP47, GRIA3/4, GAP43, synaptotagmin 2, LRFN2, SV2...
Open access
Research Article10.9734/ajpr/2024/v14i12408
Background: Pediatric infectious diseases pose a significant risk to child health worldwide. Vaccination programs have greatly reduced the incidence and severity of these diseases, though coverage and efficacy differ across regions. This mini-review examines how effectively these...
Open access
Research Article10.9734/ajpr/2024/v14i12407
Background: Asthma continues to lead to significant health issues and deaths worldwide, and there has been little progress in treatment outcomes over the past ten years, even though treatment costs have risen. Methodology: This mini review compared new therapeutic approaches for...
Open access
Research Article10.9734/ajpr/2024/v14i12406
Purpose: Choledochal cyst, a cystic dilatation of biliary tree, is a congenital abnormality of unknown etiology. Excision of cyst & biliary reconstruction is the mainstay of treatment. Most patients (80%) with choledochal cyst are detected after clinical manifestations. Major...
Open access
Research Article10.9734/ajpr/2024/v14i12405
Introduction: The incidence of T1D is increasing worldwide, particularly in young children under 6 years of age. The objective of this study was to describe the characteristics of type 1 diabetes in children under 5 years of age in our resource-limited country setting. Materials...
Open access
Research Article10.9734/ajpr/2024/v14i12404
Autism in childhood is a heterogeneous disease with around 110 phenotypes. Around 800 genes are affiliated with autism including members of neuro-ligand, neurexin, cadherin, GABA receptors, SHANK gene families, mutated UBE3 A on chromosome 15 and SNORD 116 precursor interaction....
Open access
Research Article10.9734/ajpr/2024/v14i11403
Balkisu Seidu, Nasara H. Yakubu, Felicia B. Basoglee, Gifty J. Sumani, Bawa K. Khadija, Mina Sapio, Emelia Boateng, Ayishetu Sango, Dorithy T. Angakumpo, Delilah Nonterah, Rashida Atrime, Zeinab Abubakari, Mohammed A. Kojo, Rashida A. Goribia & Sumani Yakubu·Asian Journal of Pediatric Research·2024
Introduction: Postnatal care (PNC) is crucial for both mothers and newborns, reducing maternal and neonatal fatalities. It is essential for mitigating physical and cognitive impairments, disability, and mortality. However, it is often underutilized for delivering high-quality ser...
Open access
Research Article10.9734/ajpr/2024/v14i11402
Neuropsychiatric lupus encompasses the neurological and psychiatric manifestations of systemic lupus erythematosus and presents a significant diagnostic challenge due to its broad clinical variability. Affecting between 14% and 75% of lupus patients, it can occur at any stage of...
Open access
Research Article10.9734/ajpr/2024/v14i11401