Mateus Renon

B-306 DiGeorge Syndrome Associated With 10p Deletion: A Cytogenetic Case Report

DiGeorge Syndrome (DGS) is a rare genetic disorder classically associated with the deletion of the long arm of chromosome 22, leading to craniofacial and cardiac malformations, hypoparathyroidism, and immunodeficiency. However, rare cases with similar phenotypes have been associated with deletions involving the t...