Muscular dystrophy belongs to the hereditary, conditional diseases and is characterized by an increasing weakness of the musculature of the entire body. Depending on the form of the disease, patients gradually lose their mobility and independence. The two forms of Duchenne and Becker-Kiener are the most significant forms of muscle weakness. In the following text, … Physiotherapy for muscular dystrophy
Type Duchenne The type of muscular dystrophy after Duchenne is already evident in childhood and immobility due to the insufficiency of the skeletal muscles occurs in early childhood.Typical for the Duchenne type is the limitation in walking where the children hold their thighs when they stand up (Gowers sign). Since the course is progressive, the … Type Duchenne | Physiotherapy for muscular dystrophy
History The course is progressive in all forms of muscular dystrophy (always progressive). It begins with a weakening of the muscles in the pelvic girdle area and then spreads further. Initially, weakness in the leg muscles is noticeable, as well as difficulty in walking. Fat and connective tissue is then formed from the muscles, resulting … History | Physiotherapy for muscular dystrophy
Summary Even with the symptoms of muscular dystrophy, patients can lead an independent life. For example, even with the Becker-Kiener form, the patient can reach a high age, whereas Duchenne patients have lower life expectancies. In order to provide the patient with an individual therapy in both forms, physiotherapy can be prescribed. Thus, the muscle … Summary | Physiotherapy for muscular dystrophy
Mendel’s laws are fundamental laws of heredity (genetics). Heredity is the transmission of traits and characteristics from parents to subsequent generations. The Augustinian priest, teacher and geneticist Johann Gregor Mendel (1822 – 1884) was the first researcher to methodically investigate the rules of heredity and is known as the “founder of heredity”. He was unaware … What are Mendel’s Laws?
What is the breast cancer gene? The development of breast cancer (mamma carcinoma) can have many different causes. In some cases it can be traced back to a gene mutation. However, it is assumed that only 5-10% of breast cancer cases are based on a hereditary genetic cause. In this case one speaks of hereditary … The breast cancer gene
What does it mean for me if I have this gene? As mentioned above, women with a positive family history should be closely monitored and possibly tested. Before deciding on a molecular genetic diagnosis, the pros and cons should be weighed up and the limits of the diagnosis and possible consequences should be considered. It … What does it mean for me if I have this gene? | The breast cancer gene
How is the breast cancer gene inherited? The inheritance of the BRCA-1 and BRCA-2 mutation is subject to a so-called autosomal dominant inheritance. This means that the BRCA mutation present in one parent is passed on to the offspring with a 50% probability. This occurs independently of gender and can also be inherited from the … How is the breast cancer gene inherited? | The breast cancer gene
Introduction Colon cancer is one of the most common cancers in adults. On the one hand, it poses a great danger, but on the other hand, the screening programmes and treatment options for this disease are promising. Most people are diagnosed with colorectal cancer at an advanced age. It is not unusual for it to … Is colon cancer hereditary?
What can I do to prevent the onset of hereditary colorectal cancer? Numerous test procedures and regular examinations are offered for the prevention of hereditary intestinal cancer syndromes. The most important known syndromes can already cause initial changes in childhood. The FAP syndrome, for example, can already be accompanied by polyps from the age of … What can I do to prevent the onset of hereditary colorectal cancer? | Is colon cancer hereditary?
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
Hyperactivity, attention deficit hyperactivity syndrome, ADHD, attention deficit disorder with hyperactivity, fidgeting syndrome, attention deficit hyperactivity disorder. Attention Deficit Syndrome, Psychoorganic Syndrome (POS), Hyperkinetic Syndrome (HKS), Behavioural Disorder with Attention and Concentration Disorder. English: Attention-Deficit-Hyperactiv-Disorder (ADHD), minimal brain syndrome, Attention – Deficit – Hyperactivity – Disorder (ADHD), Fidgety Phil. ADHS, attention deficit syndrome, Hans-guck-in-the-air, Attention-Deficit-Disorder … Causes of ADHD
