People who travel a lot can contract cutaneous leishmaniasis, a disease of the skin and mucous membranes for which there is no vaccine and which can be severe with a number of complications. It is also popularly known as Oriental bump. Vacationers should therefore prevent it as best they can and seek medical attention if … Cutaneous Leishmaniasis: Causes, Symptoms & Treatment
Congenital dyserythropoietic anemias (CDA) are very rare congenital disorders characterized by ineffective hematopoiesis. The first symptoms of anemia appear in childhood. These diseases can be treated quite well by various therapeutic measures. What is congenital dyserythropoietic anemia? Congenital dyserythropoietic anemias belong to a group of rare blood disorders caused by different gene mutations. In the … Congenital Dyserythropoietic Anemia: Causes, Symptoms & Treatment
Diaphragmatic palsy, or phrenic paralysis, results from paralysis of the phrenic nerve. It originates in the third to fifth cervical segments of the spinal cord and activates the diaphragm as well as several other organs in the chest cavity, such as the pericardium. Paralysis of the nerve causes the diaphragm on the affected side to … Diaphragmatic Paresis: Causes, Symptoms & Treatment
We talk about twins or multiples when instead of one expected baby, two, three or more children are born at once. However, multiple pregnancies are not without risk. What are twins and multiples? According to the Hellin rule, one in 85 pregnancies is a twin pregnancy. Multiple pregnancies with at least two children are considered … Twins and Multiples: Function, Tasks, Role & Diseases
Arachidonic acid belongs to the polyunsaturated fatty acids. It is semiessential for the body. Arachidonic acid is found predominantly in animal fats. What is arachidonic acid? Arachidonic acid is a quadruply unsaturated fatty acid and belongs to the omega-6 fatty acids. Omega-6 fatty acids serve as precursors to prostaglandins and thus play an important role … Arachidonic Acid: Function & Diseases
Biotinidase deficiency is a very rare inherited metabolic disorder. It occurs due to a genetic defect in the enzyme biotinidase. About one in 80,000 children is born with such an enzyme disorder. Newborn screening helps to make the diagnosis. What is biotinidase deficiency? Biotinidase deficiency, or BTD for short, belongs to the group of rare … Biotinidase Deficiency: Causes, Symptoms & Treatment
