Thrombocytopenias and thrombocytopathies distinguishing features in Morocco while typological aspects taking into consideration

Abstract

Disturbances in morphological-functional thrombocytic indices are met rather often in Morocco. The disorders can be primary or hereditary and secondary or acquired as well as quantitative and qualitative. The authors analyzed ethnic, ethnic-gender, ethnic-age and ethnic-gender-age typological aspects contribution in platelets’ structural-functional peculiarities in the Moroccans. They paid attention to thrombocytopenias and thrombocytopathies peculiarities in Morocco taking typological aspects into consideration. Materials and methods: A literary review of scientific sources for 2020-2025 concerning to platelets pathologies in Morocco. Quantitative (Willebrand disease, congenital amegakaryocytic thrombocytopenia, platelets’ integrin receptors anomalies, constitutional thrombocytopeny, idiopathic thrombocytopeny, immune thrombocytopeny) and qualitative problems (Glanzmann thrombasthenia) with platelets were found to be representing serious health issues in Morocco with significant positive correlation of their development to typological aspects.