Brief overview Marfan syndrome Diagnosis: A suspected diagnosis usually results from the findings of the physical examination; genetic testing is necessary to confirm the diagnosis. Prognosis: Life expectancy is often normal nowadays, but regular check-ups, especially with a cardiologist, are very important. Symptoms: Changes in the heart, especially dilatation of the aorta, changes in the … Marfan Syndrome: Symptoms, Life Expectancy
Marfan syndrome is an inherited disease of the connective tissue. Left undiagnosed, Marfan syndrome can cause sudden death and the number of undiagnosed cases is still estimated to be high. The genetic disease is considered incurable, and treatment options are also very limited, always aiming to improve the quality of life of those affected. What … Marfan Syndrome: Causes, Symptoms & Treatment
Finger deformities occur relatively rarely. They are either inherited or occur as spontaneous mutations, which are then also passed on to the offspring. In addition, finger abnormalities can be the result of accidents. They are usually not very noticeable externally, such as camptodactyly, unless they are severe cases of deformity. What is camptodactyly? Camptodactyly is … Camptodactyly: Causes, Symptoms & Treatment
Hypermobility syndrome (HMS) is characterized by excessive flexibility of the joints caused by congenital connective tissue weakness. Little is known about the cause of the condition. Quality of life is particularly limited by chronic pain in the joints. What is hypermobility syndrome? Hypermobility syndrome is a connective tissue weakness that leads to unusual overmovement of … Hypermobility Syndrome: Causes, Symptoms & Treatment
Endocarditis Prophylaxis Endocarditis prophylaxis is an antibiotic cover for minor surgical procedures such as tooth extraction. This is intended to prevent the development of a dangerous inflammation of the inner wall of the heart in heart-damaged patients. In the past, the need for such antibiotic coverage was much broader. However, data have shown that the … Endocarditis Prophylaxis | Mitral valve prolapse
Definition A mitral valve prolapse is a protrusion and protrusion of the so-called mitral sail into the left atrium. The mitral valve is one of the four valves of the human heart and is most frequently affected by abnormalities and diseases. One speaks of a mitral valve prolapse when the valve protrudes more than 2mm … Mitral valve prolapse
Complaints For a long time a protrusion of the mitral sail does not cause any complaints. Especially if the bulge is not yet so strong that the blood flow is impaired, patients usually do not notice the valve damage. However, as soon as the mitral leaflet is bulged so far that it reaches directly into … Complaints | Mitral valve prolapse
Treatment The treatment depends on several factors. For example, the most important decision on whether or not treatment should take place depends on the severity of the valve prolapse. In most cases, a protrusion of the mitral leaflet is discovered only by chance and the actual valve damage does not cause any discomfort or impairment. … Treatment | Mitral valve prolapse
Is a mitral valve prolapse dangerous? Per se, mitral valve prolapse is not dangerous because it does not have a dangerous effect on blood distribution and supply in the body for a long time. The greatest danger is an untreated and worsening mitral valve prolapse. Because if this valve damage is not treated, there is … Is a mitral valve prolapse dangerous? | Mitral valve prolapse
Heredity is responsible for making children resemble their relatives. Within the framework of complex processes, various characteristics are passed on to descendants via the chromosomes. In the process, two expressions for each trait always meet through the mother and father. What is heredity? Humans have 46 chromosomes. Chromosomes are carriers of DNA, on which all … Heredity: Function, Tasks, Role & Diseases
As mentioned above, Marfan Syndrome is a genetic disorder. An alteration (mutation) of the Fibrillin-1 (FBN-1) gene causes a defect in the microfibrils (structural component of connective tissue) and weakening of the elastic fibers, which manifests itself mainly in the organ systems of the heart, skeleton, eye and vessels. Autosomal dominant inheritance means that an … Signs of Marfan syndrome
Synonyms in a broader sense Type 1 fibrillopathy; arachnodactyly syndrome; spider finesse; Achard-Marfan syndrome; MFA Marfan syndrome is a rare, genetic disease of connective tissue with abnormal changes in the heart, vessels, eye and skeleton with the leading symptom of long, narrow or spider limb. The basis of Marfan syndrome is a mutation of the … Marfan syndrome