Aomar Agadr
Mohammed V University
46 Papers
52 Citations
Aomar Agadr is an academic researcher from Mohammed V University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 4, co-authored 31 publications.
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Papers
Von Willebrand's disease: case report and review of literature.
TL;DR: A case of infant in 27-month-old boy who had been referred due to haemorrhagic shock showed unfortunately, the most severe form of Von Willebrand's Disease; Type 3.
Vitamin B12 deficiency: case report and review of literature.
Brahim El Hasbaoui,Nadia Mebrouk,Salahiddine Saghir,Abdelhkim El Yajouri,Rachid Abilkassem,Aomar Agadr +5 more
TL;DR: The early diagnosis and treatment of vitamin B12 deficiency is crucial for significant neurological impairment and long-term prognosis as discussed by the authors, which is an important cause of neurodevelopmental delay and regression.
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Grisel's syndrome: a rare complication following traditional uvulectomy.
TL;DR: Clinicians should be aware of acute nontraumatic torticollis if patient had a recent surgery in the head or neck area or undergone an upper respiratory tract infection when treating patients with Grisel's syndrome.
Macrophage activation syndrome associated with griscelli syndrome type 2: case report and review of literature.
TL;DR: A case of Macrophage activation syndrome associated with Griscelli syndrome type 2 in a 3-years-old boy who had been referred due to severe sepsis with non-remitting high fever, generalized lymphoadenopathy and hepato-splenomegaly is presented.
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DNA ligase IV deficiency: Immunoglobulin class deficiency depends on the genotype.
Rodolphe Dard,Bérénice Hervé,Thierry Leblanc,Jean-Pierre de Villartay,Laura C. Collopy,Tom Vulliami,Séverine Drunat,Stephanie Gorde,Abel Babik,Pierre-François Souchon,Aomar Agadr,Rachid Abilkassem,Mustapha Elalloussi,Alain Verloes,Martine Doco-Fenzy +14 more
TL;DR: Clinical presentation ranges in severity from rapidly fatal to mild hemato-immunological forms associated with microcephalic developmental delay, and genome instability results in a broad range of Onco-Hemato-Immunological disturbances.
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