Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
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Authors
H Jelti
Department of Medical Genetics and Oncogenetics, Mohammed VI University Hospital center, Tangier, Morocco
Life and Health Sciences Laboratory, Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Assaadi University, Morocco
K Khabbache
Department of pediatrics, Mohammed VI University Hospital center, Tangier, Morocco
Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Assaadi University, Morocco
S Bouressas
Department of Medical Genetics and Oncogenetics, Mohammed VI University Hospital center, Tangier, Morocco
Life and Health Sciences Laboratory, Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Assaadi University, Morocco
F Hacht
Department of Medical Genetics and Oncogenetics, Mohammed VI University Hospital center, Tangier, Morocco
Life and Health Sciences Laboratory, Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Assaadi University, Morocco
A Oulmaati
Department of pediatrics, Mohammed VI University Hospital center, Tangier, Morocco
Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Assaadi University, Morocco
A Lamzouri
Department of Medical Genetics and Oncogenetics, Mohammed VI University Hospital center, Tangier, Morocco
Life and Health Sciences Laboratory, Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Assaadi University, Morocco
DOI: https://doi.org/10.2478/bjmg-2025-0006 | Journal eISSN: 2199-5761
Language: English
Published on: Oct 8, 2025
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 times per year
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© 2025 H Jelti, K Khabbache, S Bouressas, F Hacht, A Oulmaati, A Lamzouri, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.