First Case of H Syndrome in Northern Morocco: Clinical Features and Literature Overview
By: H Jelti, A Lamaibdel, S Bouressas, M Benkacem, S Regragui and A Lamzouri
Authors
Department of Medical Genetics and Oncogenetics, Mohammed VI University Hospital, Tangier, Morocco
Life and Health Sciences Laboratory, Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Essaâdi University, Morocco
A Lamaibdel
Department of Medical Genetics and Oncogenetics, Mohammed VI University Hospital, Tangier, Morocco
Life and Health Sciences Laboratory, Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Essaâdi University, Morocco
S Bouressas
Department of Medical Genetics and Oncogenetics, Mohammed VI University Hospital, Tangier, Morocco
Life and Health Sciences Laboratory, Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Essaâdi University, Morocco
M Benkacem
Department of endocrinology, Mohammed VI University Hospital, Tangier, Morocco
S Regragui
Department of Hematology, Mohammed VI University Hospital, Tangier, Morocco
A Lamzouri
Department of Medical Genetics and Oncogenetics, Mohammed VI University Hospital, Tangier, Morocco
Life and Health Sciences Laboratory, Faculty of Medicine and Pharmacy of Tangier, Abdelmalek Essaâdi University, Morocco
DOI: https://doi.org/10.2478/bjmg-2026-0004 | Journal eISSN: 2199-5761 (formerly 1311-0160) | Journal ISSN: 1311-0160
Language: English
Page range: 81 - 86
Published on: Oct 14, 2026
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
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© 2026 H Jelti, A Lamaibdel, S Bouressas, M Benkacem, S Regragui, A Lamzouri, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution 4.0 License.