ABMGG LGG Practice Questions - ABMGG Laboratory Genetics And Genomics (LGG) Exam

Access More Questions

A chromosomal microarray (CMA) reveals a 3 Mb deletion at 22q11.2 in a child with conotruncal heart defect and palatal abnormalities. What is the most likely diagnosis?

Williams syndrome DiGeorge syndrome / 22q11.2 deletion syndrome Angelman syndrome Smith-Magenis syndrome

Correct Answer:

DiGeorge syndrome / 22q11.2 deletion syndrome

Access more questions from this quiz

Continue to ABMGG LGG Practice Questions - ABMGG Laboratory Genetics and Genomics (LGG) Exam for more practice questions and the full quiz experience.

Access More Questions