What FAMILIAL PERIODIC PARALYZES means: Familial Periodic Paralyzes - are a group of inherited neurological disorders caused by mutations in genes that regulate sodium and calcium channels in nerve cells. They are characterized by episodes in which the affected muscles become slack, weak, and unable to contract. Between attacks, the affected muscles usually work as normal. Treatment of the periodic paralyzes focuses on preventing further attacks and relieving acute symptoms. Avoiding carbohydrate-rich meals and strenuous exercise, and taking acetazolamide daily may prevent hypokalemic attacks.
- Definition Fabry Disease:
- Dictionary caused by the lack of or faulty enzyme needed to metabolize lipids, fat-like substances that include oils, waxes, and fatty acids. The enzyme is known as ceramide trihexosidase, also called alpha familial periodic paralyzes.
- Definition Fahr'S Syndrome:
- Dictionary Syndrome - also known as Idiopathic Basal Ganglia Calcification or Fahr's Syndrome is a rare, genetically dominant, inherited neurological disorder characterized by abnormal deposits of calcium familial periodic paralyzes.
- Definition Fainting - Also Called Syncope:
- Dictionary called Syncope, is a sudden, and generally momentary, loss of consciousness, or blacking out caused by the Central Ischaemic Response, because of a lack of sufficient blood and oxygen in the brain familial periodic paralyzes.
- Definition Floppy Infant Syndrome - Also Known As Hypotonia Or Infantile Hypotonia:
- Dictionary Syndrome - also known as hypotonia or infantile hypotonia, a condition of abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle familial periodic paralyzes.