Bartter syndrome is an inherited renal tubular disorder caused by a defective salt reabsorption in the thick ascending limb of loop of Henle. It characterized by urinary loss of sodium, potassium, and chloride; hypokalemic metabolic alkalosis; normal blood pressure, high plasma l...
Open access
Research Article10.9734/ajpr/2020/v4i430153
Tanvir Kabir Chowdhury, S. M. Humayun Kabir, Md. Abdullah Al Farooq, Md. Khurshid Alam Sarwar, Rajib Khastagir & Md. Minhajuddin Sajid·Asian Journal of Pediatric Research·2020
Aims: While the developed world has significantly reduced mortality from surgical conditions in children, there is lack of adequate data on the outcome of children’s surgical conditions in the developing world. This study aims at assessing the spectrum of mortalities from childre...
Open access
Research Article10.9734/ajpr/2020/v4i330151
Background: The most vulnerable period of life to develop seizures is the neonatal period. These events very often signify serious damage or malfunction of the immature developing central nervous system. Neonatal seizures may arise as a result of diverse etiologies and can have v...
Open access
Research Article10.9734/ajpr/2020/v4i330152
Introduction: Infant bronchiolitis is the most common acute viral infection infection of the lower respiratory tract in children. Many pharmacological interventions have been suggested, including bronchodilators, yet the efficacy of bronchodilators in the treatment of this infec...
Open access
Research Article10.9734/ajpr/2020/v4i330150
Background: Bioelectrical analysis measures two bioelectrical vectors: Resistance (R) and reactance (Xc). Resistance is the pure opposition of a biological conductor to the flow of an alternating current through the intra and extra-cellular ionic solution and it is inversely rela...
Open access
Research Article10.9734/ajpr/2020/v4i330149
Alagille syndrome is a multi-systemc genetic disorder with variable phenotypic penetrance that was first described in 1969 by Daniel Alagille.It is characterized by anomalies of the intrahepatic bile ducts, heart, eye and skeleton, which are associated with facial features . The...
Open access
Research Article10.9734/ajpr/2020/v4i330148
Objective: To study the effect and safety of Fenofibrate in uncomplicated hyperbilirubinemia in newborn with 6-month follow-up. Materials and Methods: This is a randomized controlled clinical trial conducted in 60 normal term neonates admitted for uncomplicated hyperbilirubinemia...
Open access
Research Article10.9734/ajpr/2020/v4i230147
Hakan Erdogan, Ayse Cavidan Sonkur, Orhan Görükmez, Ayse Erdogan, Dilek Damla Saymazlar & Fatih Unal·Asian Journal of Pediatric Research·2020
Aim: Familial Mediterranian Fever is an autosomal recessive disease characterized by recurrent inflammatory attacks of serosal membranes. The aim of the current study was to determine the frequency of the Mediterranean fever (MEFV) gene pathogenic variants in 158 children (78 mal...
Open access
Research Article10.9734/ajpr/2020/v4i230145
Md. Abdullah Al Farooq, Mohammad Nazmul Haq, Tania Tajreen, Md. Minhajuddin Sajid & Tanvir Kabir Chowdhury·Asian Journal of Pediatric Research·2020
Objective: Although Bangladesh is rapidly gaining economic development, education and health related indices are not equally developed in all parts of the country. The objective of the study was to compare the socio-economic and health status of students in public and private pri...
Open access
Research Article10.9734/ajpr/2020/v4i230146
Neonatal jaundice is defined as the yellowish discoloration of the skin and sclera due to accumulation of unconjugated bilirubin. This is common in newborns and if not detected and treated early can lead to severe morbidity and mortality. Aim: The aim of the study was to analyze...
Open access
Research Article10.9734/ajpr/2020/v4i230144