Behind the health impairment, colloquially simply referred to as MRSA infection, there is a whole circle of symptoms that have affected and still affect a large number of inpatients in recent times and in the present. What is MRSA infection? According...
REM sleep behavior disorder (RBD) is a sleep disorder in which complex movements take place during the dream phase. The patient reacts aggressively to certain dream contents. RBD is often the precursor to Parkinson’s disease, Lewy body dementia, or MSA (multiple...
APV stands for anomalous pulmonary veins. The anomalous pulmonary venous connection represents a malfunction of the lungs. The blood is usually pumped from the veins of the lungs into the atrium on the left side. In the context of an anomalous pulmonary...
MDS stands for Miller-Dieker Syndrome. Miller-Dieker syndrome is a rare congenital developmental disorder of the brain and causes serious damage to the brain structure. Miller-Dieker syndrome is caused by a genetic defect. The disease is incurable and requires lifelong and loving care. What...
KGB Syndrome, also known as Hermann-Pallister Syndrome, is a very rare hereditary disorder that affects all body systems. The genetic disorder is characterized by unusual facial features, skeletal abnormalities, and delayed development. What is KGB Syndrome? Basically, the KGB syndrome is based...
The cauda syndrome (also called cauda syndrome) describes a pinching of the nerves in the area of the cauda equina. It is often associated with a severe herniated disc and requires immediate action when the typical symptoms appear in order to decompress the pinched...
Lambert-Eaton-Rooke Syndrome, also known as LES for short, is a very rare disorder of the nervous system. The LES belongs to the myasthenic syndromes. What is Lambert-Eaton-Rooke Syndrome? Lambert -Eaton-Rooke syndrome is also known as pseudomyasthenia. The neurological disease is very...
CD stands for Craniodiaphyseal dysplasia. Craniodiaphyseal dysplasia is a congenital skeletal disorder associated with hyperostosis and sclerosis of the facial skeleton. The cause is a genetic mutation of the bone structure-inhibiting genes. Therapy is symptomatic and focuses on stopping the progression of...
The L1CAM syndrome is a rare hereditary disease. L1CAM syndrome is inherited along an X-linked path. The typical symptoms of L1CAM syndrome are spasticity, an adducted thumb and various brain anomalies in the affected patients. What is L1CAM Syndrome? The causes...
Arthrosis of the knee joint or gonarthrosis is the most common form of arthrosis in Germany. This chronic disease belongs to the so-called rheumatic group of diseases. Its symptoms, the course of the disease and options for prophylaxis and therapy will...
