Shamsun Nahar Shanta, Afroza Begum, Syed S. Haque, Tahmina Jesmin, Abdullah-Al Mamun, Shanjida Sharmim, Ashiqur Rahman Khan & Ashraful Islam·Asian Journal of Pediatric Research·2023
Background: Idiopathic nephrotic syndrome (INS) is a common childhood illness with or without relapses. So, the objectives of this study is to find out such children who are prone to develop frequent relapse and the demographic characteristics responsible for relapse. This retros...
Open access
Research Article10.9734/ajpr/2023/v13i4304
Background: Rheumatic Heart Disease (RHD), also known as "Bouillaud's disease", is a post-streptococcal non-suppurative inflammatory disease complicating an upper airway infection with group A β-hemolytic streptococcus. Although RHD has almost disappeared in developed countries,...
Open access
Research Article10.9734/ajpr/2023/v13i4301
Mohammad Naim Iqbal Mollah, Md. Abdur Rouf, Mohammad Moniruzzaman Bhuiyan, Mohammad Sazzad Hossain Chowdhury, Azreen Chowdhury & Bilkis Sultana·Asian Journal of Pediatric Research·2023
Background: Nephrotic Syndrome (NS) is a common and recurrent glomerular disease in childhood. Although the exact etiology of NS is not fully known, it is believed that immune system plays a pivotal role in its pathogenesis. Studies have been reported a strong association between...
Open access
Research Article10.9734/ajpr/2023/v13i4299
Eman Alaqeli, Salma. Elzwai, Ahmed Atia, Fawzia Ahmed, Manal Abuagela, Najia Alwaseea, Arij Mousa, Rehab Jerbi, Abir Ben Ashur, Hamida El Magrahi & Eman Abdulwahed·Asian Journal of Pediatric Research·2023
Aims: This study aimed to determine the clinical and epidemiological profile, and outcomes of accidental poisonings in children. Study Design: This observational retrospective study. Place and Duration of Study: General ward and ICU of Benghazi Children's Hospital, from the 1st...
Open access
Research Article10.9734/ajpr/2023/v13i4300
Schizencephaly is a rare anomaly of embryonic development characterized by the presence of linear fissures containing cerebrospinal fluid and lined with dysplastic gray matter, extending from the pial surface of the cerebral hemisphere to the ependymal surface of the lateral vent...
Open access
Research Article10.9734/ajpr/2023/v13i4298
Background: Chronic Liver Disease (CLD) is a complex and often debilitating condition that affects individuals of all ages, including children. Within pediatric CLD, one critical aspect that demands careful evaluation is the presence and severity of esophageal varices. If left un...
Open access
Research Article10.9734/ajpr/2023/v13i4295
Samson Ojedokun, Taiwo Oloyede, Ayobami Alabi, Oluwaseyi Oke, Abraham Akinbola, Olawumi kofoworade & Olanike Oladibu·Asian Journal of Pediatric Research·2023
Fetal and neonatal alloimmune thrombocytopenia (FNAIT) is a rare disease resulting from the effect of maternal alloantibodies on fetal human platelet antigens HPAs which could lead to severe haemorrhage. An antibody from mother reacting against a defined platelet alloantigen has...
Open access
Research Article10.9734/ajpr/2023/v13i4296
Background: Although neonates present with critical pulmonary stenosis (PS) it is equally found in grown up children in developing country like Bangladesh. Balloon pulmonary valvuloplasty (BPV) is one of the most common catheter- based intervention. Transcatheter interventions in...
Open access
Research Article10.9734/ajpr/2023/v13i4297
Aims: This study aimed to examine the association between cord blood lipid levels and neonatal birth weight. Study Design: Hospital based prospective cross-sectional study. Place and Duration of Study: Study was conducted in Government medical College Nagpur, a tertiary care hosp...
Open access
Research Article10.9734/ajpr/2023/v13i4294
Nager syndrome, or preaxial acrofacial dysostosis, is a rare malformation characterized by abnormalities of the craniofacial skeleton and limbs. Although most cases are sporadic and some cases have been demonstrated to have an autosomal dominant or recessive mode of inheritance,...
Open access
Research Article10.9734/ajpr/2023/v13i4293