Exogenous lipoid pneumonia ELP is a rare condition in common pediatric practice. Its clinical presentation is non-specific. Delay in diagnosis and treatment exposes infants to chronic respiratory failure. We report the observation of a 2-month-old infant with respiratory signs th...
Open access
Research Article10.9734/ajpr/2024/v14i3333
In 1862, the French doctor Maurice Raynaud published his dissertation in Paris titled "Sur l’asphyxie locale et la gangrène symétrique des extrémités" (On local asphyxia and symmetrical gangrene of the extremities). In it, he described a series of cases in which there were episod...
Open access
Research Article10.9734/ajpr/2024/v14i3332
Background: Family-Centered Care is a care approach in which healthcare professionals collaborate with the patient's family to plan and make decisions regarding the patient's treatment. Family-Centered Care is widely acknowledged and documented as the optimal care approach for ne...
Open access
Research Article10.9734/ajpr/2024/v14i3331
Nowadays, as a result of an increasing proportion of families in which parents are in funded jobs, there has been a steady increase in the demand for care of young children. The present study investigated infections in childcare facility and The samples were taken by sterile cott...
Open access
Research Article10.9734/ajpr/2024/v14i3329
The purpose of a neurological examination of the newborn is to determine a normal neurological condition and to detect abnormal conditions. The examination includes assessment of the central and peripheral nervous system and observation of posture, muscle tone, strength, reflexes...
Open access
Research Article10.9734/ajpr/2024/v14i3328
The administration of intravenous levetiracetam (IV-LEV) serves as a significant therapeutic approach for managing seizures in pediatric patients. The major factors that are involved in the equation determinants contain pharmacokinetic parameters, such as dosage regimen, drug int...
Open access
Research Article10.9734/ajpr/2024/v14i3327
Apert's disease is an acrocephalosyndactyly, which is part of the craniofaciostenosis group. It is characterized by craniofacial dysmorphia and syndactyly of the hands and feet. It is a rare autosomal dominant condition, but sporadic cases are common. The pathogenesis is poorly u...
Open access
Research Article10.9734/ajpr/2024/v14i2326
Amezola Herrera Eduardo, Reyes Berlanga Mónica Lucía, Venegas Mojica Cristian Israel, Pérez Sandoval Raúl & Sánchez Villegas María del Carmen Socorro·Asian Journal of Pediatric Research·2024
Introduction: We present the case of a 5-year-old schoolboy with a cutaneous loxoscelism. Loxoscelism is defined as the clinical picture of poisoning after the bite of a spider of the genus Loxosceles. There are two well-defined medical variants: cutaneous and systemic loxoscelis...
Open access
Research Article10.9734/ajpr/2024/v14i2325
Background: Respiratory illnesses are prevalent among children, attributed to factors such as immature immune systems, anatomical variations, and increased susceptibility to infections. Acute respiratory distress syndrome (ARDS) is a significant cause of morbidity and mortality,...
Open access
Research Article10.9734/ajpr/2024/v14i2324
Inborn Errors of Immunity (IEI) is an extremely rare group of heterogenous disorders which are characterized by predisposition to severe unusual and recurrent infections, severe allergies, features suggestive of autoimmune conditions and sometimes malignancies. We report a two-ye...
Open access
Research Article10.9734/ajpr/2024/v14i2323