An Unusual Case of Headache in a Child: Idiopathic Intracranial Hypertension with Diagnostic Challenge

por Alqahtani, Youssef Ali M, Aljabri, Mohammed Fahad, Oshi, Mohammed Ahmed Mohammed, Kamal, Naglaa M, Elhaj, Waleed, Abosabie, Sara A, Abosabie, Salma AS
Publicado 2023

First report of SYNE1 arthrogryposis multiplex congenita from Saudi Arabia with a novel mutation: a case report

por Kamal, Naglaa M., Alzeky, AlaaEddin M., Omair, Maher R., Attar, Ruwayd A., Alotaibi, Abdullah M., Safar, Abdullah, Alosaimi, Nawal S., Abosabie, Sara A. S.
Publicado 2022

Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation

por Bakkar, Ayman A, Alsaedi, Abdulaziz, Kamal, Naglaa M, Althobaiti, Enad, Aboulkhair, Lujain A, Almalki, Abdullah M, Alsalmi, Shaima A, Alharthi, Qaydah, Abosabie, Sara A, Abosabie, Salma AS
Publicado 2023

Vertebral artery dissection aneurysm in a pediatric patient: A rare case with unusual clinical manifestations, diagnostic, and management challenges

por Oshi, Mohammed A. M., Aljabri, Mohammed Fahad, Alotaibi, Saad, Alzahrani, Yahea, Alfaifi, Jaber, Abosabie, Salma A. S., Abosabie, Sara A., Algethami, Samaher S., Younes, Alaa E., Almanjoomi, Raid K., Babkour,, Bashar, Kamal, Naglaa M.
Publicado 2023