Chromosomal mutations are changes to one or more chromosomes in an individual. These changes can be passed on to descendants. A consequence of such mutations may be disease, malformation, or disability. What are chromosomal mutations? Various changes are possible on a chromosome. This is because chromosomes can break apart, resulting in mutations. There are seven … Chromosomal Mutation: Causes, Symptoms & Treatment
Apert syndrome is a rare hereditary disease. Malformations occur throughout the organism with severe, chronic loss of function and disease progression through deformities. Both sexes are equally affected. What is Apert syndrome? Apert syndrome, also known as acrocephalosyndactyly syndrome, is causative of severe to very severe malformations that can affect the entire body. These multiple … Apert Syndrome: Causes, Symptoms & Treatment
Marked monoamine oxidase A deficiency is genetic and is often characterized by impulsive aggressiveness. This results in disruption of the breakdown of serotonin, epinephrine, norepinephrine, or dopamine. The gene encoding monoamine oxidase-A (MAO-A) is located on the X chromosome. What is monoamine oxidase-A deficiency? Monoamine oxidases represent enzymes responsible for the breakdown of monoamines. In … Monoamine Oxidase A Deficiency: Causes, Symptoms & Treatment
Fuhrmann syndrome is a disease that is present in affected individuals at birth. Fuhrmann syndrome is enormously rare and is one of the hereditary diseases. Typical for the Fuhrmann syndrome is a hypoplasia of the calf bone, which is called fibula in medical terminology. In addition, the fingers are affected by anomalies and the femur … Fuhrmann Syndrome: Causes, Symptoms & Treatment
Birt-Hogg-Dube syndrome is an autosomal dominant inherited disorder based on mutations in the FLCN gene. Patients suffer from multiple skin lesions, lung cysts, and renal tumors. Treatment is limited to symptomatic resection and, if necessary, follow-up of the tumors. What is Birt-Hogg-Dube syndrome? Hereditary diseases are conditions caused by mutation(s) in one or more genes … Birt-Hogg-Dube Syndrome: Causes, Symptoms & Treatment
In melorheostosis, bones of the extremities thicken completely or proportionally without patients noticing. Only in rare cases do edema of the muscles, growth disturbances, or movement restrictions become apparent. Symptomatic therapy is limited to patients with actual symptoms. What is melorheostosis? Diseases with more specified alterations in bone density or structure are a broad group … Melorheostosis: Causes, Symptoms & Treatment
Mental causes That psychological factors, such as stress, anxiety or other psychological problems, cause ulcerative colitis is not the case, even though researchers have previously assumed this. What is certain, however, is that these psychological factors clearly influence the course of the disease. For example, stress or psychological problems can lead to or negatively influence … Mental causes | Causes of ulcerative colitis
Genetic causes In ulcerative colitis, a genetic involvement of the disease can be assumed. However, it is not yet possible to say whether a single gene or several genes are involved. So far, one gene has been discovered that is suspected to be associated with ulcerative colitis. It has been found that ulcerative colitis occurs … Genetic causes | Causes of ulcerative colitis
Introduction The exact cause of ulcerative colitis, which leads to inflammation in the colon, is still unknown. It is obvious that several environmental factors play a role and the disease can be influenced by psychological stress. However, genetic factors also play a very important role, as the disease is more common in some families. Possible … Causes of ulcerative colitis
