Ghita Hachim, Abdelhakim Ourrai, Abdelilah Radi, Najat Lamalmi, Rachid Abilkassem, Rihane El Mohtarim, Amal Hassani & Aomar Agadr·Asian Journal of Pediatric Research·2022
Autoimmune Hepatitis (AIH) pathogenesis is still unknown. However, among patients who have a genetic susceptibility, some viral infections appear to be triggers for AIH. We report a case of a child who developed type 2 autoimmune hepatitis as a result of HEPATITIS A Virus (HAV) i...
Open access
Research Article10.9734/ajpr/2022/v9i230264
Sara Benchidmi, Yolande Salome Mimboe, Yasmine Lamghari, Saad Assila, Najat Lamalmi, Ghizlane Jaabouti, Sara Aminou, Ouidad Elqorchi, Naima EL. Hafidi, Chafiq Mahraoui & Soumia Benchekroun·Asian Journal of Medicine and Health·2023
Chediak Higashi syndrome (CHS) is an autosomal recessive disorder, caused by biallelic mutations in the highly conserved LYST gene. It is characterized by partial oculocutaneous albinism and immunodeficiency. Approximately 500 cases are reported worldwide. Here we report a case o...
Open access
Research Article10.9734/ajmah/2023/v21i11953
Sinus histiocytosis, also known as Rosaï Dorfman Syndrome (SRD), is a noncancerous condition that causes the growth of large masses of histiocytes in lymph nodes, primarily in the cervical area. Visceral damage is common, and diagnosis is made through histological examination. Th...
Open access
Research Article10.9734/ajpr/2023/v12i2236