Skip to content

Tag: Congenital heart defect

Explore our comprehensive collection of health articles in this category.

What Does It Mean to Have No Heart? A Look at the Medical, Emotional, and Artificial Contexts

5 min read
The total artificial heart (TAH) is a device that can temporarily take over the function of a failing human heart, allowing a person to live without their native organ. Understanding **what does it mean to have no heart** requires exploring the vast differences between this medical reality and the deep figurative meaning of the phrase, which refers to a lack of compassion or empathy.

What does it mean to maintain a patent in general health?

5 min read
In medical contexts, the term 'patent' is a diagnostic description, not a legal one, and signifies that a vessel or duct is open and unobstructed. Understanding what it means to maintain a patent in general health is crucial for interpreting medical information correctly, particularly concerning certain congenital heart defects.

What is DKS in medical terms? A Comprehensive Guide

4 min read
In medicine, acronyms can have multiple meanings depending on the context. One such abbreviation, DKS, is a prime example, referring to a major heart surgery known as the Damus-Kaye-Stansel procedure, as well as a severe diabetic complication called diabetic ketoacidosis (DKA).

What condition does Brian Littrell have?

4 min read
For decades, Brian Littrell has captivated audiences as a member of the Backstreet Boys, all while privately managing significant health issues. Learning what condition does Brian Littrell have provides insight into his remarkable resilience and longevity in the music industry.

What is the interracial septum? Understanding the Heart’s Interatrial Septum

4 min read
The human heart contains a crucial wall of tissue that separates its upper chambers. A common online misspelling, "interracial septum," often leads to a search for this vital anatomical structure, which is correctly known as the interatrial septum. This expert guide clarifies the misconception and provides a comprehensive overview of its function and importance.

What is the Noonan syndrome?

5 min read
Noonan syndrome is a genetic disorder affecting an estimated 1 in 1,000 to 2,500 births worldwide. This condition is a *RASopathy*, caused by mutations in specific genes that regulate cellular signaling during development and impacting multiple systems of the body.