Pathophysiology: The Case Study of Robert’s 22q11.2 Deletion Syndrome

Pathophysiology: The Case Study of Robert’s 22q11.2 Deletion Syndrome Robert, an 11-year-old boy, has been undergoing regular medical examinations and monitoring due to complications arising from a genetic condition. He has been diagnosed with 22q11.2 deletion syndrome, a disorder caused by a microdeletion of genetic material on chromosome 22. Individuals with this syndrome exhibit a […]

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Date: October 5th, 2023

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