Practice 20 MCQs on CONGENITAL HEART DISEASE with OmpathStudy. Built for Kenyan medical and health students to revise key concepts and prepare for exams.
Q1. At what stage of gestation does the heart and vasculature become the first fully functional organ system?
Answer: 4 weeks
Explanation: The heart and vasculature become the first fully functional organ system at approximately 4 weeks of gestation.
Q2. Which of the following is the most common genetic cause of congenital heart disease?
Answer: Trisomy 21 (Down syndrome)
Explanation: Trisomy 21, or Down syndrome, is the most common genetic cause associated with congenital heart disease.
Q3. What percentage of patients with Down syndrome have one or more heart defects?
Answer: 40%
Explanation: Approximately 40% of patients with Down syndrome have one or more heart defects.
Q4. A "shunt" in congenital heart disease is best defined as:
Answer: An abnormal communication between chambers or vessels
Explanation: A shunt refers to an abnormal communication allowing blood to flow between chambers or vessels, bypassing normal circulation.
Q5. Which condition is characterized by a "machinery-like" murmur?
Answer: Ventricular septal defect (VSD)
Explanation: Patent ductus arteriosus (PDA) is classically associated with a continuous, 'machinery-like' murmur.
Q6. Cyanosis is a primary clinical feature of which group of disorders?
Answer: Right-to-left shunts
Explanation: Cyanosis, a bluish discoloration of the skin, results from deoxygenated blood bypassing the lungs, which occurs in right-to-left shunts.
Q7. Eisenmenger syndrome occurs when:
Answer: A left-to-right shunt reverses to right-to-left due to pulmonary hypertension
Explanation: Eisenmenger syndrome is characterized by the reversal of a left-to-right shunt to a right-to-left shunt, caused by severe pulmonary hypertension.
Q8. Which of the following is NOT one of the four cardinal features of Tetralogy of Fallot?
Answer: Left atrial dilation
Explanation: The four cardinal features of Tetralogy of Fallot are overriding aorta, ventricular septal defect, right ventricular hypertrophy, and pulmonary stenosis (subpulmonic stenosis). Left atrial dilation is not a primary feature.
Q9. What is the most common form of congenital heart disease (excluding bicuspid aortic valve)?
Answer: Ventricular septal defect
Explanation: Ventricular septal defect (VSD) is the most common form of congenital heart disease, excluding bicuspid aortic valve.
Q10. The "second heart field" in fetal development primarily populates which structures?
Answer: Outflow tract, right ventricle, and most of the atria
Explanation: The second heart field contributes significantly to the formation of the outflow tract, right ventricle, and much of the atria.
Q11. Which transcription factor mutation is specifically linked to DiGeorge syndrome and neural crest migration?
Answer: TBX1
Explanation: TBX1 mutation is specifically linked to DiGeorge syndrome, which involves defective neural crest migration.
Q12. Paradoxical embolism is a potential complication of:
Answer: Right-to-left shunts (or transient reversal of left-to-right shunts)
Explanation: Paradoxical embolism occurs when an embolus from the venous system crosses to the arterial system through a right-to-left shunt, such as a patent foramen ovale or an ASD/VSD with reversed flow.
Q13. Which of these is a typical "obstructive" congenital lesion?
Answer: Coarctation of the aorta
Explanation: Coarctation of the aorta is an obstructive lesion characterized by a narrowing of the aorta.
Q14. Secundum ASDs (90% of all ASDs) result from a deficiency in the:
Answer: Septum secundum
Explanation: Secundum atrial septal defects, the most common type, are due to a deficiency in the septum secundum.
Q15. At birth, the closure of the foramen ovale is triggered by:
Answer: Decreased pulmonary vascular pressure and increased left atrial pressure
Explanation: At birth, lung expansion leads to decreased pulmonary vascular resistance, increasing pulmonary blood flow and left atrial pressure, which functionally closes the foramen ovale.
Q16. "Clubbing" of the fingers is a clinical sign associated with:
Answer: Chronic severe hypoxia/cyanosis
Explanation: Clubbing of the fingers is a sign of chronic severe hypoxia or cyanosis, often seen in cyanotic congenital heart diseases.
Q17. Most ventricular septal defects (VSDs) occur in which part of the septum?
Answer: Membranous part
Explanation: The membranous part of the ventricular septum is the most common site for VSDs.
Q18. In Tetralogy of Fallot, "subpulmonic stenosis" refers to:
Answer: Obstruction of the right ventricular outflow tract
Explanation: Subpulmonic stenosis in Tetralogy of Fallot refers to the obstruction of the right ventricular outflow tract, leading to reduced pulmonary blood flow.
Q19. Which medication is used to maintain ductal patency in certain life-threatening CHDs?
Answer: Prostaglandin E1
Explanation: Prostaglandin E1 is administered to maintain the patency of the ductus arteriosus in infants with ductal-dependent congenital heart defects.
Q20. Which syndrome involves a deletion on chromosome 22q11.2?
Answer: DiGeorge syndrome
Explanation: DiGeorge syndrome is characterized by a microdeletion on chromosome 22q11.2, leading to various developmental abnormalities including heart defects.