The Interconnected World of Dermatology and Ophthalmology by Gyanesh Rathore, Surajit Gorai, Gitikash Purkayastha, Kinnor Das, Prajwal Pudasaini

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The Importance and Deficiencies of Medical Treatment Guidelines for Genetic Disorders in the Middle East Region by Majid alfadhel

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Advancement in Gene therapy: Current and Future of Gene Therapy by Shafee Ur Rehman

Subjects: “…Genetic disorders, Global Health, Genes and Gene therapy…”
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A Case Series of Alport Syndrome with Posterior Lenticonus by Sumit Navneet Toshniwal, OK Radhakrishnan, Nikhil Toshniwal, Priyanka Aher, Deepaswi Bhavsar

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Genetic aspects of nonimmune hydrops fetalis by H. A. Sarkisyan, S. V. Dumova, E. I. Shabelnikova, A. A. Fadeeva, K. S. Zizyukina, I. Yu. Zyablova, A. P. Khokhlova, O. I. Savateeva, D. M. Muscherova, I. V. Zhuravleva

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Awareness and attitudes of pregnant women concerning genetic disorders and pregnancy termination in northeastern Iran by Nafiseh Todarbary, Abouzar Irandegani, Mojtaba Meshkat, Aida Gholoobi, Tayebeh Hamzehloei

Subjects: “…Genetic disorders…”
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A comprehensive report of the clinical and mutational profiles of 30 Iranian malignant infantile osteopetrosis patients by Akbar Amirfiroozy, Maryam Naghinejad, Azim Rezamand, Hamid Farhangi, Zahra Golchehre, Hossein Jalali, Mohammad Taheri, Mohammad Keramatipour

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Frequency Analysis of Genetic Disorders Among Probable Carriers Identified Through Premarital Screening in Behshahr, 2023 by Mojgan Geran, Zahra Kashi, Mohammad Khademloo, Saman Soudmand arshad, Rogheye Khatoon Arab, Maryam Zarrinkamar

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Unlocking the potential: advancements and applications of gene therapy in severe disorders by Rahul G. Ingle, Gehan M. Elossaily, Mohd Nazam Ansari, Shivani Makhijani

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A first large study of whole-exome sequencing (WES) in 489 patients with suspected rare genetic disorders at a tertiary centre in Malaysia by Lip Hen Moey, Go Hun Seo, Boon Eu Cheah, Wee Teik Keng, Hane Lee, Gaik Siew Ch’ng

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Pathogenic variation underlying rare diseases in an Arab population: Implications for screening programs by Ruchi Jain, Sami Bizzari, Sathishkumar Ramaswamy, Khaleem F. Hasham, Shruti Sinha, Ikram Chekroun, Fatma Rabea, Eman Abuijlan, Maha El Naofal, Massomeh Sheikh Hassani, Shruti Shenbagam, Alan Taylor, Mohammed Uddin, Mohamed Almarri, Omer Alkhnbashi, Hamda Khansaheb, Hanan Al Suwaidi, Stefan S. Du Plessis, Stephany El-Hayek, Alawi Alsheikh-Ali, Ahmad Abou Tayoun

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Not All Neonatal Encephalopathies Are due to Perinatal Hypoxia by Tushar Kulkarni, Lma Dsougi Hussein Mohamed, Mahmoud El Halik, Fatma Abdulla Mohammad Bastaki

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Hereditary kidney disease with auditory abnormalities: analysis of mutations and clinical phenotypes by Jingru Bi, Wenkai Guo, Pengcheng Ji, Yuansheng Xie

Subjects: “…Genetic disorders…”
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Clinical Characteristics of Multiple Café-Au-Lait Macules and Their Potential Significance in the Early Screening of Genetic Diseases by Chen T, Wu J, Yang X, Xia Z, Yang R

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Personalized Medicine in Treating Rare Genetic Disorders: A Review by Ansari Zebanaz, Affan M. Kareem, Ashwini A. Aher, Sunil N. Thitame

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Neuromuscular diseases: genomics-driven advances by Anna Cho

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Triangular Lunulae in Papillon–Lefèvre Syndrome: A Case Report by Zarak Khan Shiraz, Fahad Faizullah, Qaisar Ali Khan, Irfan Ullah, Mehran Khan, Bader Semakieh, Zain Ul Islam, Ravina Verma

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Concurrent Variants in SLC29A3 and EFL1 Genes Presenting as Infantile Onset Transfusion-dependent Anaemia in a Child: A Case Report by D Karthik, Pramila Gopal Menon, Parag Tamhankar, Shailaja Mane, Dnyaneshwar Upase

Subjects: “…genetic disorders…”
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Systematic Review of Management Strategies for Alport Syndrome: Implications for Male Patients by Zouina Sarfraz, Ayesha Khan, Maryyam Liaqat, Aden Khan, Faheem Javad, Meher Saleem, Azza Sarfraz, Musfira Khalid, Muzna Sarfraz, Manish Kc, Omar Irfan

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Cardiovascular Diseases in Public Health: Chromosomal Abnormalities in Congenital Heart Disease Causing Sudden Cardiac Death in Children by Cecilia Salzillo, Marco La Verde, Amalia Imparato, Rossella Molitierno, Stefano Lucà, Francesca Pagliuca, Andrea Marzullo

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