Glutaric aciduria type 1: a review of phenotypic and genetic characteristics by Ali M AlAsmari, Mohammed M Saleh, Abdul Ali Peer-Zada

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Harel-Yoon syndrome: the first case report from Saudi Arabia by Alaa AlAyed, Manar A. Samman, Abdul Ali Peer-Zada, Mohammed Almannai

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Clinical laboratory and radiological findings in COVID-19 patients with variable severity: King Fahad Medical City experience by Shaeeb Mustafa, Abdul Ali Peer-Zada, Faisal AlAsmari, Asiya Wali, Husam Sakkijha

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Atypical presentation of adenosine deaminase 2 deficiency with bi‐allelic ADA2 mutation by Reem Al‐shaikh, Dimah Alnowaiser, Abdul Ali Peer‐Zada, Awatif Almutairi, Hamza Alghamdi

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Novel de novo heterozygous CACNA1A gene variant in generalised dystonia: a case report by Shahad Bawazeer, Mohammed Alshareet, Aljoharah Alakkas, Omar A Alsinaidi, Abdul Ali Peer-Zada

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Outcome of cerebral venous thrombosis in a critically Ill COVID-19 infected patient: A case report by Shaeeb Mustafa, Abdul Ali Peer-Zada, Faisal AlAsmari, Asiya Wali, Husam Sakkijha

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Favorable outcome of PML‐RARα short isoform and FLT3‐ITD mutation in a patient with several adverse prognostic markers: A case report by Mohammed A. Bafail, Rahaf AlTahan, Manar A. Samman, Suha A. Tashkandi, Ibraheem H. Motabi, Abdul Ali Peer‐Zada

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Neurological and extra-neurological clinical spectrum observed in pediatric patients with EMC1 gene variants identified by whole exome sequencing by Abdul Ali Peer-Zada, Osama A. Obaid, Manar A. Samman, Aqeela AlHashim, Hajar AlAsmari, Ali M. AlAsmari

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A rare presentation of BCR‐ABL1 and RUNX1‐MECOM rearrangement in a pediatric patient with acute myeloid leukemia by Ragdah M. Alamri, Maryam Alanazi, Rajeh K. AlRajeh, Suha A. Tashkandi, Azizah F. Alswayyed, Manar A. Samman, Abdul Ali Peer‐Zada

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