X-Linked Adrenoleukodystrophy in a Moroccan Patient: Genetic Diagnosis Leads to Presymptomatic Testing and Family Counseling
By:
Authors
M Mansouri
Genetic department, Research Clinical Center, Mohammed VI University Hospital, Marrakech
Childood, Health and Development Research Center, Faculty of Medicine, Cadi Ayyad University
T Smol
Institut de Génétique Médicale, CHU Lille, Lille, France
N Louhabe
Neurology Department, Mohammed VI University Hospital, Faculty of Medicine, Cadi Ayyad University, Marrakech
M Rama
Institut de Génétique Médicale, CHU Lille, Lille, France
N Rada
Pediatric Department, Mohammed VI University Hospital, Faculty of Medicine, Cadi Ayyad University, Marrakech
N Fdil
Metabolic platform, Biochemistry Laboratory, Team for Childhood, Health and Development, Faculty of Medicine, Cadi Ayyad University
M Bouskraoui
Pediatric Department, Mohammed VI University Hospital, Faculty of Medicine, Cadi Ayyad University, Marrakech
N Aboussair
Genetic department, Research Clinical Center, Mohammed VI University Hospital, Marrakech
Childood, Health and Development Research Center, Faculty of Medicine, Cadi Ayyad University
DOI: https://doi.org/10.2478/bjmg-2025-0002 | 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 M Mansouri, T Smol, N Louhabe, M Rama, N Rada, N Fdil, M Bouskraoui, N Aboussair, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.