The 22q11.2 Deletion Syndrome in Congenital Heart Defects
The 22q11.2 deletion syndrome is amongst the most common microdeletion syndrome in humans. Its prevalence remains unknown in sub-Saharan Africa, and its clinical features are under-reported for people of African descent.
Source: CVD Prevention and Control - Category: Global & Universal Authors: Ambroise Wonkam, Ricardo Toko, David Chelo, Cedrik Tekendo-Ngongang, Samuel Kingue, Sophie Dahoun Tags: Original Research Source Type: research
More News: African Health | Cardiology | Heart | International Medicine & Public Health | Microdeletion Syndromes