The following Conditions are related to Seizures

Select a specific condition below to view its details.

  • Autosomal dominant long qt syndrome

    Many people who have long QT syndrome don't have any signs or symptoms. You might be aware of your condition only because of: Results of an electrocardiogram (ECG) done for an unrelated reason A family history of long QT syndrome Genetic testing results Fainting is the most common sign of long QT syndrome. Fainting (syncope) occurs when the heart temporarily beats in an unorganized way  Read More

  • Jervell and lange-nielsen syndrome

    Jervell and Lange-Nielsen syndrome is a rare genetic illness characterized by congenital deafness that occurs in conjunction with anomalies in the heart's electrical system. The severity of JLNS-related cardiac symptoms varies among individuals. Some people have no symptoms (asymptomatic); others develop abnormally fast heartbeats (tachyarrhythmias), which can cause bouts of unconsciousness, cardiogenic shock, and potential  Read More

  • Neonatal lupus erythematosus

    Neonatal lupus erythematosus (NLE) is a rare but serious condition that can affect newborns. It's important to know what the risk factors are so that you can take steps to protect your baby and prevent NLE.The most common risk factor for NLE is being born to a mother who has had lupus, or having one or more family members who have lupus. However, not all babies born to mothers with lupus develop NLE—i  Read More

  • Sneddon syndrome

    Sneddon syndrome is a rare, progressive blood vessel disease. Specifically, arteries transports pure blood away from the heart and into the body. It is largely characterized by net-like patterns of discoloration on the skin (livedo reticularis) and neurological problems caused by artery obstructions. It usually affects older adults, and the clinical manifestations starts with old age. Individual differences in symptoms and sev  Read More

  • Taybi syndrome

    Taybi syndrome is a rare genetic condition that develops due to some genetic disorders. It starts to make its presence in early childhood, characterized by deformity in facial features, intellectual impairment, and abnormal physical structure. The condition affects both males and females equally. However, in most cases, the diagnosis of the syndrome is random with the absence of family members with  Read More