Introduction: Adams-Oliver's syndrome (SAO) is a rare genetic condition characterized by the association of lumb anomalies and Aplasia cutis congenita in vertex, often accompanied by underlying ossification defect and vascular lesions. The objective through this new observation i...
Open access
Research Article10.9734/ajpr/2023/v13i4313
Nesma Ghareeb ElBaioumy, Walid Ahmed ElShehaby, Amany Mohammed ElGharib, Lamia Morad & Abeer Abdelrahman ElToukhy·Asian Journal of Pediatric Research·2023
Background: Congenital heart defects are the singular most common congenital anomalies and account for a significant fraction of childhood mortality and morbidity. Hearing impairment was the most frequent sensory deficit. Auditory brainstem response (ABR) was determined to assess...
Open access
Research Article10.9734/ajpr/2023/v13i4309
Background: Transient tachypnea of the newborn (TTN) is a prevalent etiology of respiratory distress (RD) in neonates. The condition is a result of the accumulation of fetal lung fluid owing to defective processes responsible for its removal. However, differentiating TTN from var...
Open access
Research Article10.9734/ajpr/2023/v13i4310
Like every other prevalent disease process, cardiovascular diseases pose a great risk for the morbidity and mortality of human beings. Pediatric cardiovascular disease (CVD) represents a broad spectrum of disorders that affect both the heart and blood vessels in the pediatric pop...
Open access
Research Article10.9734/ajpr/2023/v13i4308
Background: The child and adolescent obesity have become a major public health problem. Selenoprotien p1 (SEPP1) is widely acknowledged to be among the most delicate functional indicators of Se status and it plays a role in the metabolism of Se and in anti-oxidative defense. So...
Open access
Research Article10.9734/ajpr/2023/v13i4306
Congenital Adrenal Hyperplasia (CAH) comprises a set of inherited conditions marked by enzymatic deficiencies within the adrenal steroidogenesis pathway, resulting in compromised cortisol synthesis and, in certain instances, heightened androgen production. Congenital adrenal hype...
Open access
Research Article10.9734/ajpr/2023/v13i4307
Background: Neonatal respiratory distress one of the main causes of neonatal morbidity and mortality. It is a diagnostic and therapeutic emergency whose etiology is dominated by respiratory pathologies. Objective: To study the epidemiological, clinical, diagnostic, therapeutic, a...
Open access
Research Article10.9734/ajpr/2023/v13i4305
Kisito Nagalo, Balkissa Konaté, Sonia Douamba, Ralph Eden Idogo, Aïssatou Bélemviré, Myriam Sanwidi, Carine Kyélem & Diarra Yé·Asian Journal of Pediatric Research·2023
Objective: To gain a better understanding of congenital malformations and to help reduce neonatal morbidity and mortality, particularly in a context of resource-limited countries. Methods: This descriptive cross-sectional study with retrospective and prospective data collection o...
Open access
Research Article10.9734/ajpr/2023/v13i4303
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