Can DiGeorge Syndrome be Cured?
No
Management addresses specific symptoms and complications
What is DiGeorge Syndrome?
DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a genetic disorder that can affect various organs and systems. It may lead to heart defects, immune system issues, and developmental delays. Treatment addresses specific symptoms and complications.
Clinical Aspects
Characteristics
Genetic disorder causing immune system and facial abnormalities
Symptoms
Immune issues, heart defects, facial features
Diagnosis
Genetic testing, clinical evaluation
Prognosis
Variable, depends on the severity of organ involvement
Complications
Complications affecting multiple organs
Etiology and Treatment
Causes
Chromosome 22 deletion
Treatments
Supportive care, surgeries as needed
Prevention
Supportive care, surgeries as needed
Public Health and Patient Perspectives
Epidemiology
Genetic disorder characterized by the absence or underdevelopment of certain structures
Patient Perspectives
Supportive care, management of associated conditions
For personalized advice and care, always seek the assistance of healthcare professionals. This information is meant for general understanding and not as a replacement for professional medical advice.
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