Disease, lipid storage
Disease, lipid storage: A series of disorders due to inborn errors in lipid metabolism resulting in the abnormal accumulation of lipids in the wrong places (Examples include Gaucher, Fabry and Niemann-Pick diseases and metachromatic leukodystrophy).
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- Disease, Lobstein's
Disease, Lobstein’s: Osteogenesis imperfecta type I. An inherited, generalized connective tissue disorder featuring bone fragility and blue sclerae (blue whites of the eyes). The classic mild form of “brittle bone disease.” It is a dominant trait with males and females affected. One copy of the mutant gene is sufficient to cause the disease. Clinically it […]
- Disease, Lou Gehrig
Disease, Lou Gehrig: Amyotrophic lateral sclerosis (ALS), a classic motor neuron disease. Motor neuron diseases are progressive chronic diseases of the nerves that come from the spinal cord responsible for supplying electrical stimulation to the muscles. This stimulation is necessary for the movement of body parts. LOU GEHRIG’S DISEASE: Amyotrophic lateral sclerosis is quite a […]
- Disease, manic-depressive
Disease, manic-depressive: See Manic depression. The antiquated term for bipolar disorder.
- Disease, maple syrup urine
Disease, maple syrup urine: Hereditary disease due to deficiency of an enzyme involved in amino acid metabolism, characterized by urine that smells like maple syrup. The three branched-chain amino acids: (leucine, isoleucine, and valine) cannot be metabolized (processed) and build up in the blood to the detriment of brain function. Untreated maple syrup urine disease […]
- Disease, Meniere
Disease, Meniere: A condition with recurrent vertigo accompanied by ringing in the ears (tinnitus) and deafness. Symptoms include vertigo, dizziness, nausea, vomiting, loss of hearing (in the affected ear), and abnormal eye movements. Meniere disease is due to dysfunction of the semi-circular canals (endolymphatic sac) in the inner ear. The treatment of Meniere disease usually […]