Brief overview Treatment: Depending on the trigger, for example in the case of fatty liver, abstinence from alcohol and change of diet; according to the underlying disease, possibly medicinal or surgical therapy. Causes: Alcohol abuse, overeating, viral diseases, metabolic diseases, cholestatic diseases, vascular diseases, certain drugs, liver cysts, tumors. When to see a doctor: In … Hepatomegaly: Causes, Signs, Treatment
Osteosclerosis describes a hardening of the bones due to various causes. In this process, there is an excessive increase in bone substance. However, the stability of the bones is impaired. What is osteosclerosis? Osteosclerosis is not a single disease. The term describes only the changes in bone toward hardening and increase in bone mass. Despite … Osteosclerosis: Causes, Symptoms & Treatment
Porphyria cutanea tarda, or PCT, is the most common form of porphyria. Symptoms mainly affect the skin and liver. The disease is readily treatable, although the underlying disorder is incurable. What is porphyria cutanea tarda? Porphyria cutanea tarda is one of the so-called porphyrias and, in fact, is the most common subtype of these disorders. … Porphyria Cutanea Tarda: Causes, Symptoms & Treatment
Truncus arteriosis communis is the name given to a very rare heart defect in newborns caused by incomplete separation of the pulmonary arterial trunk from the arterial trunk of the systemic circulation. The aorta and pulmonary artery arise in a common trunk, resulting in mixing of the oxygen-depleted arterial blood of the pulmonary circulation with … Truncus Arteriosus Communis: Causes, Symptoms & Treatment
Biliary atresia is the narrowing of the bile ducts that occurs during development in the womb. Causes of such are largely unknown, though links to certain viral diseases have been identified through research. Disease is manifested by prolonged jaundice after birth, colorless stools, brown-colored urine, an enlarged liver and later spleen enlargement, water retention and … Biliary Atresia: Causes, Symptoms & Treatment
Aortic isthmic stenosis is a congenital heart defect. It involves a narrowing of the aorta. What is aortic isthmic stenosis? Aortic isthmic stenosis (coarctatio aortae) is the second most common type of congenital heart defect. In this case, a luminal narrowing of the aorta (main artery) occurs in the region of the aortic isthmus (isthmus … Aortic Isthmus Stenosis: Causes, Symptoms, & Treatment
Caroli disease is the name given to a rare disease of the bile ducts. In it, affected individuals often suffer from inflammation and gallstones in the bile ducts. What is Caroli disease? Caroli disease is a very rare bile duct disease that is already congenital. It involves a marked dilatation of the large bile ducts … Caroli Disease: Causes, Symptoms & Treatment
Pulmonary valve regurgitation is a relatively rare condition of the heart valve, which is usually a symptom of disease. In very few cases, pulmonary valve regurgitation requires therapy; however, in severe disease, surgery is possible, so a heart valve replacement is needed. What is pulmonary valve regurgitation? Doctors speak of pulmonary valve insufficiency when the … Pulmonary Valve Regurgitation: Causes, Symptoms & Treatment
Acute lymphoblastic leukemia, or ALL, is an acute form of leukemia caused by malignant lymphocyte precursor cells. It mostly affects children. The cure rate is approximately 50% in adults and 80% in children. What is acute lymphoblastic leukemia? Acute lymphoblastic leukemia, or ALL, is an acute form of leukemia caused by malignant lymphocyte precursor cells. … Acute Lymphoblastic Leukemia: Causes, Symptoms & Treatment
Cholerstinester storage disease is a lysosomal storage disease and inborn error of metabolism with a genetic basis. The disease is hereditary and is caused by a genetic mutation in the coding genes for lysosomal acid lipase. Symptomatic treatment of patients is conservative medication or enzyme replacement therapy steps. What is cholesterol ester storage disease? The … Cholesterol Ester Storage Disease: Causes, Symptoms & Treatment
Juvenile myelomonocytic leukemia is a malignant form of leukemia that occurs in infants and young children. In many cases, Juvenile Myelomonocytic Leukemia is simply referred to by the abbreviation JMML. In Juvenile Myelomonocytic Leukemia, malignant transformation of hematopoietic stem cells, which are precursors of monocytes, occurs. What is juvenile myelomonocytic leukemia? Basically, juvenile myelomonocytic leukemia … Juvenile Myelomonocytic Leukemia: Causes, Symptoms & Treatment
Juvenile idiopathic arthritis is a chronic joint disease that belongs to the rheumatic group. It occurs before the age of 16 and lasts at least six weeks. What is juvenile idiopathic arthritis? Juvenile idiopathic arthritis, also known as Still’s disease, is also known by the synonym juvenile rheumatoid arthritis. It is abbreviated JIA and JRA, … Juvenile Idiopathic Arthritis: Causes, Symptoms & Treatment
