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Embryological Basis of Atrial Septal Defect

Development and Fusion of Septum Primum and Septum Secundum

Atrial septal defect results from improper fusion of the septum primum and septum secundum during fetal development, affecting blood flow between atria.

6/7/20256 min read54 views
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Embryological Basis of Atrial Septal Defect Explained

Embryological Basis of Atrial Septal Defect

Introduction

Atrial septal defect (ASD) is a congenital heart condition arising due to abnormalities in the development of the septum primum and septum secundum.

Development of Septum Primum

The septum primum forms during early fetal development, growing from the roof of the atrium and extending downward. Initially, an opening called the ostium primum exists, which later closes as the septum fuses with endocardial cushions.

Development of Septum Secundum

As the septum primum develops, another muscular structure, the septum secundum, begins to grow adjacent to it. This growth process leaves an opening known as the foramen ovale, which allows fetal blood to bypass the lungs.

Fusion Process and Atrial Septal Defect

Normally, at birth, the septum primum and secundum fuse, closing the foramen ovale. However, incomplete fusion results in an atrial septal defect, leading to abnormal blood flow between atria.

Types of Atrial Septal Defect

  • Ostium Secundum Defect – The most common form, arising from incomplete formation of the septum secundum.
  • Ostium Primum Defect – Associated with endocardial cushion abnormalities.
  • Sinus Venosus Defect – Located near the entry of the superior vena cava.

Clinical Implications

ASD can lead to complications such as right heart overload, pulmonary hypertension, and arrhythmias. Early diagnosis and management are crucial.

Conclusion

Understanding the embryological basis of ASD helps in better diagnosing and treating the condition. Advances in medical research continue to improve outcomes.

Tags

#Atrial Septal Defect#Septum Primum#Septum Secundum#Congenital Heart Defect#Embryology

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