Introduction: Digestive involvement is not uncommon during chronic inflammatory diseases in children, it may be just digestive manifestations other than other systemic signs or association of two different pathologies with a common immunological terrain. Objective: To recognize t...
Open access
Research Article10.9734/ajpr/2022/v10i1189
Solitary mastocytoma is the most common form of mastocytosis in children. The main symptom is pruritus. The treatment is symptomatic and it’s based on Topical corticosteroids. The prognosis is good with possibility of spontaneous regression at adulthood. This case report is about...
Open access
Research Article10.9734/ajpr/2021/v6i330194
Summary: Rasmussen's encephalitis (RE) is a rare and severe chronic inflammatory brain disease resulting in drug-resistant epilepsy and progressive hemispheric destruction with neurological deficit. ER is associated with deterioration of background EEG activity, progressive atrop...
Open access
Research Article10.9734/ajpr/2023/v13i3284
The case report is being done to increase the knowledge of Congenital Cystic Adenomatoid Malformation (CCAM) along with to better understand about the disease and its management & raise awareness. A female infant (aged 9 months and birth weight 2500 gm) was selected as partic...
Open access
Research Article10.9734/ajpr/2023/v13i2257
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
Factor XIII deficiency is a rare inherited disease, with a particularly high risk of intracerebral hemorrhage. We report the case of a newborn who was suspected to have a coagulation disorder at birth, due to an intracerebral hemorrhage. A quantitative dosage of factor XIII was r...
Open access
Research Article10.9734/ajpr/2021/v6i130187