Diseases

Wolman's disease is a lysosomal storage disease that is inherited in an autosomal recessive manner. In the disease there is a loss of the activity of the so-called lysosomal acid lipase. Wolman's disease comes

A pancreatic tumor can be benign or malignant, with the majority of all diagnosed tumors in the pancreas being malignant. While benign tumors can be removed relatively easily, malignant tumors or pancreatic carcinomas are

Paget's disease is a disease of the skeleton that is also known as osteodystrophia deformans. In Paget's disease, the bone metabolism is disturbed, resulting in thickening of the bones. Paget's disease sufferers

Hyponatremia is when the level of sodium in the blood is too low. It is one of the most common electrolyte disorders.

Drooping upper eyelids, also known as drooping eyelids, make the face look older and tired. Often there is also a medical indication when those affected decide to have an operation. From Blepharochalasis

The Costello syndrome is an autosomal dominant inherited undesirable development. Characteristic features are developmental delays, intellectual disability, cardiac abnormalities, and gross facial features.

Kabuki syndrome, also known as Kabuki make-up syndrome or Niikawa-Kuroki syndrome, is a very rare hereditary disease. The cause is so far unknown; the therapy is concerned with relieving symptoms. So far there are neither rich

Pseudoxanthoma elasticum (PXE) is a rare hereditary disease also known as Grönblad-Strandberg syndrome. It mainly affects the skin, eyes and blood vessels.

The cardio-facial-cutaneous syndrome is a very rare genetic disease. It is characterized by the appearance of various physical and mental impairments. The disease can only be treated symptomatically.

Alternans syndromes are brain stem syndromes that cause crossed symptoms of paralysis and are mostly due to strokes in the area of ​​the brain stem. Possible causes are also tumors or inflammatory processes in these regions. The

Renal anemia is kidney-related anemia that can be attributed to erythropoiesis disorders (synthesis of red blood cells) caused by renal insufficiency. The extent of renal anemia will depend on the severity of the underlying

As a severe developmental disorder of the brain, lissencephaly is not curable today. The main therapeutic steps are to relieve symptoms.

The blue diaper syndrome is a congenital metabolic disease with the main symptom tryptophan malabsorption. The lack of absorption by the intestine results in a conversion and excretion via the kidneys, so that the urine turns blue. The

Hypertriglyceridemia is a disorder of lipid metabolism that manifests itself in increased triglyceride levels (triacylglycerides) in the blood of over 200 ml / dl. The disease can be genetic, caused by unfavorable external circumstances

Shoulder joint inflammation (humeroscapular periarthritis) is a degenerative disease of the shoulder or shoulder girdle. Typical signs are a restriction of mobility in the shoulder area and severe pain

Osteoarthritis or joint degeneration is a disease of the joints. In doing so, irreversible joint damage occurs primarily through persistent incorrect loading. Osteoarthritis can also occur due to cartilage defects and injuries.

In our latitudes it is quite possible to get infected with a fish tapeworm. The danger is particularly great with uncooked, raw fish that you have caught yourself.

Sinusitis, or sinusitis, is inflammation of the lining of the sinuses. It is mostly triggered by viruses or bacteria and can take an acute or chronic form. Typical symptoms are runny nose and stinging

Noise sensitivity is a high level of sensitivity to everyday sounds that are not a problem for healthy people. It is often the result of trauma, stress, or other injury.

In medical jargon, chronic sinusitis is a permanent sinus infection. It is caused by an infection of the nose with viruses or bacteria and can be treated with various drugs