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Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review Cover

Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review

Balkan Journal of Medical Genetics
Volume 28 (2025): Issue 1 (June 2025)
By: H Jelti,  K Khabbache,  S Bouressas,  F Hacht,  A Oulmaati and  A Lamzouri  
Open Access
|Oct 2025

Authors

H Jelti

houda.jelti@etu.uae.ac.ma

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
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Language: English
Published on: Oct 8, 2025
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Epileptic encephalopathy,
IER3IP1,
MEDS1,
Microcephaly,
Neonatal diabetes,
Neurodevelopmental disorder
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 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.

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