Moyamoya Syndrome as a Severe Cerebrovascular Complication of Mucopolysaccharidosis Type I: Clinical Presentation and Underlying Mechanisms

Authors

Karima Daghor-Abbaci Internal medicine department, Bab El Oued University Hospital center, Bab El Oued city, Faculty of Medicine, University of health sciences, Algiers, Algeria https://orcid.org/0000-0002-5669-5759 (unauthenticated)
Radhia Ait Chalal Radiology department, Bab El Oued University Hospital center, Bab El Oued city, Faculty of Medicine, University of health sciences, Algiers, Algeria
Hind Arzour Nephrology Department, Mustapha Bacha University Hospital Center, University of health sciences, Algiers, Algeria
Assia Haddouche Rheumatology department, Benaknoun University Hospital center, Faculté of Medicine, University of health sciences, Algiers, Algeria
Houria Saoula Department of Hepato-gastro-enterology, Bab El Oued University Hospital center, Bab El Oued city, Algiers, Algeria
Nazim Laraba Internal medicine department, Bab El Oued University Hospital center, Bab El Oued city, Faculty of Medicine, University of health sciences, Algiers, Algeria

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