DiGeorge Syndrome

DiGeorge syndrome is a congenital disorder of genetic origin that can affect the development of several organs, among them the body's defenses, the heart, and the glands that regulate calcium.

Possible manifestations: More frequent infections than usual, heart alterations present from birth, particular facial features and, at times, low calcium levels.

Underlying cause: It is due to the absence of a small fragment of genetic material, which alters the formation of certain structures during development.

Whom to consult: The internist, together with pediatricians, cardiologists, and immunologists depending on each case, takes part in the comprehensive evaluation of these patients. If there is suspicion due to repeated infections or associated findings, a coordinated medical evaluation makes it possible to organize appropriate care.