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ZTTK syndrome (Zhu-Tokita-Takenouchi-Kim syndrome) is a rare multisystem disease caused in humans by a genetic mutation of the SON gene. Common symptoms include developmental delay and often light to severe intellectual disability .
Its applications include assessment of myocardial ischemia and viability, cardiomyopathies, myocarditis, iron overload, vascular diseases, and congenital heart disease. [5] It is the reference standard for the assessment of cardiac structure and function, [6] and is valuable for diagnosis and surgical planning in complex congenital heart ...
Pre-excitation syndrome: Romano–Ward syndrome: Scimitar syndrome: Shone's syndrome: Short QT syndrome: Sick sinus syndrome: Taussig–Bing syndrome: double outlet right ventricle (DORV) and subpulmonic VSD. a cyanotic congenital heart defect: Timothy syndrome: Townes–Brocks syndrome: Triploid syndrome: Turner syndrome: VACTERL syndrome ...
The same report showed that, as of 2019, the age-adjusted death rate from heart disease was 165 per 100,000 in Black women compared to 129.6 per 100,000 in white women.
A physician may recommend cardiac imaging to support a diagnosis of a heart condition. Medical specialty professional organizations discourage the use of routine cardiac imaging during pre-operative assessment for patients about to undergo low or mid-risk non-cardiac surgery because the procedure carries risks and is unlikely to result in the change of a patient's management. [1]
The use of the term cardiac syndrome X (CSX) can lead to the lack of appreciation of how microvascular angina is a debilitating heart related pain condition with the increased risk of heart attack and other heart problems. Women may have difficulty accessing the specialist care of a cardiologist for this reason. [citation needed]
Asplenia with cardiovascular anomalies, also known as Ivemark syndrome and right atrial isomerism, [1] is an example of a heterotaxy syndrome. These uncommon congenital disorders are characterized by defects in the heart, spleen and paired organs such as the lungs and kidneys.
Arrhythmogenic cardiomyopathy (ACM) is an inherited heart disease. [1] ACM is caused by genetic defects of parts of the cardiac muscle known as desmosomes, areas on the surface of muscle cells which link them together. The desmosomes are composed of several proteins, and many of those proteins can have harmful mutations.