Who Discovered It

Also called epidemic parotitis, mumps is a common disease that affects numerous people all over the world. Even after the introduction of a special vaccine to help control this viral disease, it continues to inflict pain and discomfort to many individuals, specifically on those who are living in third world countries. In addition to the possible causes, symptoms as well as treatment for this condition, it is interesting to know more about its history including information on who discovered mumps. The Discovery of Mumps Who discovered mumps? Based on historical accounts, an American pathologist by the name of Ernest William Goodpasture was the one who discovered mumps virus in 1934. One of the major signs of this medical problem is the swelling of the salivary glands, which is accompanied by pain. Although the symptoms are not severe in children, it can lead to subfertility or infertility to men and teenage males. Aside from him, a certain C. Johnson is also credited for the discovery...

The chickenpox vaccine was created by Michiaki Takahashi in 1974. Since 1995, it has been used to immunize people from the disease. Another vaccination is required five years after the first one. There are also other treatments available to treat and relieve the symptoms. Discovery and History The illness was first described by the Persian scientist Muhammad ibn Zakariya ar-Razi (865-925). Before his discovery, chickenpox was considered to be the same as measles. Another pioneer in chickenpox research was Giovanni Filippo (1510-1580), who called it varicella. It was Richard Morton who first called the disease chickenpox. The work of William Heberden in 1767 showed how different chickenpox was from smallpox. The works of these people were crucial in bringing to light facts about chickenpox. Their studies allowed doctors to devise treatments for the disease. Signs and Symptoms The disease is caused by the varicella zoster virus (VZV). The most conspicuous symptom is a skin rash. These appear...

In ancient times, most civilizations dealt with diseases and medical problems with the use of magic or occult practices. However, there were early records that Egypt treated diseases with basic medical know-how. And an Egyptian could well be the first person who discovered heart disease and provided some medical remedy. Ebers Papyrus Georg Ebers was not who discovered heart disease. However, he discovered a 110-page or 20-meter long scroll in hieratic Egyptian inscription around 1873 to 1874 in Thebes. It was a record of medical data made and kept by ancient Egyptians in 1550 B.C. Among its contents was how to detect heart failure. The Ebers Papyrus reflects a comprehensive Egyptian knowledge of the basics of heart failures and diseases and simple measure on how to treat them. With this fact, it would be safe to assume that the first heart doctor was an Egyptian. Some Early Clinical Heart Diagnoses The Ebers Papyrus described several clinical heart diagnoses made by the early Egyptians,...

Marked by the human body’s inability to stop coagulation or blood clotting, hemophilia is a serious disease affecting numerous individuals all over the world. This condition refers to a set of hereditary genetic disorders. Aside from the possible causes, symptoms and treatments for this medical condition, it is also interesting to know its history including who discovered hemophilia. The Discovery of Hemophilia Who discovered hemophilia? A physician from Philadelphia in Pennsylvania named John Conrad Otto was the very first to discover this genetic disorder in 1803. He described the condition as hereditary, which affected males more compared to females. He then tried to track the source of the disease, who then found his way to a woman who lived in Plymouth some time in 1720. In 1828, the term ‘hemophilia’ was first used at the University of Zurich in Switzerland. Additional Facts and Other Important Information This disease was prominent in European royalty, the main reason why...

Also called by the name Alpert’s syndrome, Apert syndrome is a congenital disease wherein the feet, hands, face and skull of the patient are suffering from malformations. This disorder is primarily a form of acrocephalosyndactyly. The areas usually affected by this branchial arch syndrome are the mandible, the precursor of the maxilla and the first branchial arch. To have a clearer picture of this disease, it is good to know who discovered Apert syndrome. Read more