leptin

leptin A hormone produced mainly by adipocytes (fat cells) that is involved in the regulation of body fat. Leptin interacts with areas of the brain that control hunger and behavior and signals that the body has had enough to eat. A small number of people have genetic mutations in the leptin gene, leading to a…

leprosy

leprosy An infectious disease of the skin, nervous system, and mucous membranes that is caused by the bacteria Mycobacterium leprae. Leprosy is transmitted via person-to-person contact. For thousands of years leprosy was one of the world’s most feared communicable diseases because the nerve and skin damage often led to terrible disfigurement and disability. Today leprosy…

Lemierre’s disease

Lemierre’s disease A rare, potentially lethal complication of tonsillitis caused by anaerobic (not requiring oxygen) bacteria including Fusobacteria. The disease usually develops after a bacterial infection has created an abscess near the tonsils. Deep in the abscess, the anaerobic bacteria can flourish. The bacteria penetrate from the abscess into the neighboring jugular vein in the…

leishmaniasis

leishmaniasis A parasitic disease that is spread by the bite of sand flies infected with the protozoa Leishmania. There are several forms of leishmaniasis, the most common being cutaneous and visceral leishmaniasis (known as kala-azar). The cutaneous form of the disease causes skin sores and is usually named for a geographic place (for example, Jericho…

leiomyosarcoma

leiomyosarcoma A malignant tumor that originates in smooth muscle, the major structural component of most hollow internal organs and the walls of blood vessels. Leiomyosarcoma can occur almost anywhere in the body but is most frequently found in the uterus and gastrointestinal tract. Complete surgical excision, if possible, is the treatment of choice.

Leigh’s disease

Leigh’s disease A rare, inherited disorder characterized by degeneration of the central nervous system. Leigh’s disease can be caused by mutations in mitochondrial DNA or by deficiencies of an enzyme called pyruvate dehydrogenase. Symptoms usually begin between the ages of 3 months and 2 years and progress rapidly. Early symptoms may include poor sucking ability…