The aortic valve can be narrowed as a side effect of various conditions. It gives rise to numerous heart problems when the degree of narrowing turns severe enough to harm the flow of blood from the left ventricle to the arteries. Neglected, it can cause heart failure. Aortic valve stenosis is three times more common in men than women. Cure/medications for Aortic Valve Stenosis The only cure for Aortic Valve  Read More

Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is a recessive disorder with congenital deafness and long-QT syndrome. This disorder is a form of long QT syndrome.Symptoms of Autosomal recessive long-QT syndrome may be apparent during early childhood.Sensorineural hearing loss is usually profound, affecting both ears; however, it tends to affect the hearing of high frequencies more than low fr  Read More

Emery-Dreifuss muscular dystrophy (EDMD) or emery-dreifuss syndrome is a rare, often slowly progressive genetic disorder affecting the skeletal and cardiac muscles that make up the arms, legs, face, neck, spine, and heart. The following can determine your susceptibility to EDMD:Age: Rarely does EDMD start before age five, with the average onset age falling between five and ten years.Genetic mutations: E  Read More

Endocardial fibroelastosis is a rare genetic disorder that affects the valves of the heart, causing them to thicken and stiffen. The thickening and stiffening can lead to heart failure, arrhythmias, blood clots, and other serious complications.Fortunately, there are risk factors for endocardial fibroelastosis that you can be aware of to help you identify and prevent this condition.Risk factors for endocardial fibroelast  Read More

Heart failure is a condition when the heart is unable to pump enough blood to the body and operate effectively. As blood moves into the heart and body more slowly for a variety of reasons, the heart may not be able to pump sufficient oxygen and nutrients to fulfill the body's needs. The following are some symptoms of heart failure: • Having trouble focusing or being less alert, • Abdominal swelling, • Irregular or  Read More

Complicated cyanotic cardiac defects and asplenia affect the body's immune system. This enhances the susceptibility of newborns to fatal infections. Multiple factors play a role in the development of the Ivemark syndrome. The exact causes of Ivemark syndrome are still unknown. Sporadic cases are mainly evident. The factors causing the disorder are:Genetic factors: Ivemark syndrome is caused by genetic alteration  Read More

Surdo Cardiac syndrome - Jervell and Lange-Nielsen is a rare genetic disorder that causes abnormal electrical impulse passage in the heart. It is most common during fetal development as a result of a genetic mutation, and it can cause arrhythmias, fainting, seizures, and cerebral palsy. Although there is no cure, treatments are available to help manage symptoms and prevent complications.The severity of these sympto  Read More

One of the rare disorders with birth in an infant (maximum males) is called Thoracoabdominal Syndrome. Due to its association with all the crucial blood-vessel that connect parts of the heart and abdomen, it affects the area from the lungs, spine, and breastbone to the abdominal area and intestines. •Furthermore, it is linked with the defect of the diaphragm (the most significant respiratory musc  Read More

Velocardiofacial syndrome (VCFS) is a genetic disorder that affects the brain and body. It can cause mild to severe medical problems, such as heart defects, hearing loss, cleft lip or palate, developmental delays, and learning disabilities.The disorder is caused by changes in chromosome 22 (one of the 23 pairs of chromosomes found in each cell), which is called a deletion. This means that part of the chromosome has  Read More