Background: Vitamin D, affecting many tissues and organs of the body. It exerts many of its effects through contact with Vitamin D receptor (VDR) It Is Important especially in immune system; Immune thrombocytopenia is one of the most common causes of symptomatic thrombocytopenia...
Open access
Research Article10.9734/ajpr/2021/v7i230209
Aim: To assess the association of mother’s literacy status with infant & young child feeding (IYCF) practices and nutritional status of urban under 5 year children. Methods: A community based cross- sectional study was carried out among 356 urban children under 5 years from 3...
Open access
Research Article10.9734/ajpr/2021/v7i130208
Hypothyroidism is the condition of thyroid hormone deficiency. It can be primary or acquired. Primary hypothyroidism can be congenital or late onset. The symptoms of congenital hypothyroidism may go unnoticed in newborns if undiagnosed. Untreated, hypothyroidism can lead to poor...
Open access
Research Article10.9734/ajpr/2021/v7i130207
Aortopulmonary window (APW) is an uncommon congenital cardiac malformation, accounting for 0.1% of all congenital cardiac diseases. It is a defect between the ascending aorta and the trunk of the pulmonary artery. Such abnormality may occur as an isolated lesion or it can be asso...
Open access
Research Article10.9734/ajpr/2021/v7i130206
Angela Chia-Chen Chen, Elizabeth Reifsnider, Lihong Ou, Steven Samrock, Renuka Vemuri, Lance Lim, Gail Hock & Davis Lu·Asian Journal of Pediatric Research·2021
Aims: Human papillomavirus (HPV) infection is the most common sexually transmitted infection globally. Vaccination is effective in preventing HPV-associated cancers and is recommended for children at ages 11-12; however, the vaccination rate is suboptimal. Credible information ab...
Open access
Research Article10.9734/ajpr/2021/v7i130205
Background: Posterior urethral valve (PUV) is the most common obstructive anomaly of the urethra. Urethral valves have a wide range of clinical and anatomical presentations and today most patients are diagnosed in the prenatal or early neonatal period. Cold knife and diathermy fu...
Open access
Research Article10.9734/ajpr/2021/v7i130204
Background: Sickle cell disease is an inherited disorder of hemoglobin. It poses a public health problem in Senegal and mainly affects children and adolescents. Infections are the main cause of morbidity and mortality in children with sickle cell disease. The objective of our wor...
Open access
Research Article10.9734/ajpr/2021/v6i430203
Our study included 60 children with diabetes. We divided them into two groups: Group A and Group B. Patients assigned to Group A had controlled diabetes and formed our “Control Group”, while Group B was for patients with poorly controlled diabetes. This study was conducted in « T...
Open access
Research Article10.9734/ajpr/2021/v6i430201
Introduction: Wolcott-Rallison syndrome is a rare autosomal recessive disorder characterized by neonatal diabetes in consanguineous families. associated with liver dysfunction, epiphyseal dysplasia, and. growth retardation. It is caused by mutations in the gene encoding eukaryoti...
Open access
Research Article10.9734/ajpr/2021/v6i430202
Primary distal renal tubular acidosis (dRTA) is a rare genetic disease characterized by distal tubular dysfunction leading to metabolic acidosis and alkaline urine. It is associated with impaired acid excretion by the intercalated cells in the renal collecting duct. dRTA is dev...
Open access
Research Article10.9734/ajpr/2021/v6i430200