Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (SECISBP2) gene mutation in a pediatric patient by Lina Almohammadi, Lama Alsayel, Mohammad Aljumaa, Raghad Alhuthil, Afaf Alsagheir, Afaf Alsagheir

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Case Report: De novo DHX37 mutations in Saudi patients with 46,XY differences of sex development by Abeer Alabduljabbar, Sara Abid, Dania Farooq, Sara Aljazaeri, Yara Khamag, Raghad Alhuthil, Latifah Alfahad, Afaf Alsagheir, Afaf Alsagheir

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Prevalence and risk factors of thrombosis in patients with congenital hyperinsulinism: a retrospective analysis by Mohammed Hady Albitar, Nida Mariyam, Ziad Alhosainy, Raghad Alhuthil, Marah Nayfeh, Maeen Aldamouni, Seba Albitar, Afaf Alsagheir, Afaf Alsagheir

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Hyperinsulinism–hyperammonemia syndrome associated with GLUD1 gene mutation: a case series by Miral M. Abdulghfar, Afaf Alsagheir, Ismail A. Abdullah, Raghad Alhuthil

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Long-term outcomes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a retrospective study from a tertiary care center in Saudi Arabia by Haneen Aldalaan, Afaf Alsagheir, Nujud Alghamdi, Raghad Alhuthil, Maha Almslam, Mohamed H. Al-Hamed

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Growth Parameters in Children with Non-syndromic Cleft Lip and Palate versus Healthy Controls: A Cohort Study from Riyadh, Saudi Arabia by Fadiah Alkhattabi, Aziza Aljohar, Atheer Alharbi, Munirah Alsalman, Raghad Alhuthil, Alaa Almuabyedh, Afaf Alsagheir, Ebtisam Aljarba

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Pycnodysostosis: a case series of eight Saudi patients with cathepsin K gene mutation and a literature review by Afaf Alsagheir, Raghad Alhuthil, Ahmad T. Alissa, Faisal Joueidi, Ahmed G. Sayed, Waleed Al-Amoudi, Alanoud S. Alabdulhadi, Bassam Bin-Abbas, Bassam Bin-Abbas

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