Dictionary

When fechtner syndrome is a platelet defect. The cause lies in a mutation in the genetic make-up: Affected parents can pass the syndrome on to their children. What is Fechtner Syndrome? According to Theinternetfaqs, Fechtner syndrome is a hereditary disease…
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When fazioskapulohumeralen muscular dystrophy is a so-called dystrophic disease of the muscles. The disease begins in the majority of cases in the area of the face and the shoulder girdle. Facioscapulohumeral muscular dystrophy is a relatively rare disease. It occurs…
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The facial paralysis or facial paralysis is that allows the paralysis of the 7th cranial nerve (facial nerve) the movement of the facial muscles. The paralysis usually shows on one side, typical is a drooping corner of the mouth and…
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Favism occurs because of a defect in the G6PD gene, which codes for an important enzyme in the human body. The enzyme deficiency leads to anemia and hemolysis and cannot be treated causally. The prognosis is very good if those…
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Many people suffer from indefinable leaden fatigue for which no precise cause can be found. This chronic fatigue is known as exhaustion syndrome or fatigue syndrome. What is Fatigue Syndrome? According to Photionary, the term fatigue syndrome (French “tiredness”, “exhaustion”)…
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As fatigue in cancer, a severe depletion condition is referred to, which is not resolved by recreation and relaxation measures. More than 75 percent of all cancer patients describe fatigue with cancer as very stressful. The word “fatigue” is derived…
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In nodular fasciitis, nodular and fibroblastic growths that correspond to benign tumors form on the fascia. According to speculations, these are reactive processes after trauma or inflammation of the tissue. The differentiation from malignant diseases is particularly difficult for the…
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The farmer’s lung occurs mainly in people who deal professionally with plant debris. These include, for example, hay, straw and dry fodder. If left untreated, it can become chronic and lead to death. What is a farmer’s lung? According to…
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The Farber’s disease is caused a very rare metabolic disease that severe physical impairments and leads to death. Newborns only become ill if both parents are carriers of the same defective gene. As there is no specific therapy for the…
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The color blindness is one of the color vision problems and can be congenital or acquired. Color vision disorders, sometimes also called color vision disorders, include color vision impairment and the various forms of color blindness. The congenital color blindness…
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In the Fanconi-Bickel syndrome is a disease in which the storage is impaired glycogen. The disease is very rare and is synonymous with glycogenosis type XI or Bickel-Fanconi glycogenosis. The disease is based on a defect in the ‘GLUT-2’ gene….
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According to Growtheology, the hereditary disease Fanconi anemia occurs in very rare cases. Under appropriate circumstances, the disease can be cured. What is Fanconi Anemia? As Fanconi anemia, an inherited form of anemia (in medicine anemia hereinafter). As part of…
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When familial Mediterranean fever (FMF) is a hereditary disorder that occurs particularly in the Eastern Mediterranean region. It is a rare disease, but it is more common in some populations. The disease with sporadic attacks of fever can trigger amyloidosis….
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In the familial adenomatous polyposis is a disorder that takes place their inheritance autosomal dominant manner. The colon is attacked by polyps, which lead to colon cancer. What is familial adenomatous polyposis? According to Foodezine, familial adenomatous polyposis (FAP) is…
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The diffuse B-cell lymphoma is the most common malignant neoplasms of the lymphatic system. B-cell lymphomas belong to the group of non-Hodgkin lymphomas. What is diffuse B-cell lymphoma? Abbreviated as DBCL on abbreviationfinder, diffuse B-cell lymphoma starts from the mature…
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Probably each of us has felt the unpleasant sensations that a bad stomach triggers on our own body. Sudden pressure and bloating in the stomach, nausea, vomiting and eventually leading to facilitate vomiting are the signs of acute gastritis point….
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In medicine, the Crane-Heise syndrome is a complex of malformations, which mainly consist of insufficient ossification of the skull and aplasia of the vertebrae. The syndrome is due to a hereditary mutation that is based on an autosomal recessive inheritance….
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The Brown-Sequard syndrome is a rarely occurring disease that occurs normally by spinal cord injuries. The patient can perceive neither pain nor temperature on one side of the body. Only rarely is it the so-called pure Brown-Séquard syndrome; in many…
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The CHARGE syndrome is a genetic disease with a wide range of symptoms and clinical pictures. A colomb of the eye, heart defect, atresia of the choans, reduced length growth and development delay, genital abnormality and an abnormality of the…
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The Chorea Minor, also known as Sydenham chorea is occurring a neurological autoimmune disease that usually a few weeks after an infection with beta-hemolytic group A streptococci. The disease is usually a late manifestation of rheumatic fever. What is Chorea…
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In a asthenopia is a visual discomfort, which is caused by eyestrain due to internal and external influences. This so-called eye fatigue is not yet a disease, but if it persists it can lead to an eye disease in the…
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The Asphyxiating Throaxdysplasie is a Kurzripp-polydactyly syndrome. The patient’s narrow thorax usually causes thoracic respiratory insufficiency. If those affected survive the first two years, the risk of death in the future is reduced enormously. What is asphyxiating thoracic dyplasia? According…
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The actinomycosis is a bacterial infection that leads to abscess formation in deeper tissues. The infection is caused by bacteria of the species Aktinomyces. Medicinal and sometimes surgical intervention is used to treat the disease. What is actinomycosis? Actinomycosis is…
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The Aarskog syndrome or Aarskog-Scott syndrome is named after the pediatrician Charles I. Jr. Scott or after the human geneticist Dagfinn Aarskog. It is a very rare X-linked syndrome. This malformation syndrome is very often associated with short stature. What…
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An allergic vasculitis is a chronic inflammation of the blood vessels that lead to major organs. The causes of the disorder are unclear and there is no cure. The symptoms can be controlled with medication. What is allergic vasculitis? Allergic…
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