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What is another name for hyperkalemic periodic paralysis?
Hyperkalemic PP is also called potassium-sensitive PP.
What is the current status of research for periodic paralysis?
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What is the difference between hypokalemic and hyperkalemic periodic paralysis?
Hypokalemic periodic paralysis is characterized by low levels of potassium in the blood during attacks, leading to muscle weakness or paralysis. In contrast, hyperkalemic periodic paralysis is characterized by high levels of potassium during episodes, resulting in muscle stiffness or weakness. Both conditions are genetic and involve dysfunction in ion channels that regulate potassium levels in muscle cells.
How does the gene for hyperkalemic periodic paralysis present?
The gene for hyperkalemic PP affects virtually all who inherit it, with no difference in male-vs.-female expression.
What does the normal gene responsible for hyperkalemic periodic paralysis responsible for?
The normal gene is responsible for a muscle protein controlling the flow of sodium during muscle contraction.
What is another name for hyperkalemic periodic paralysis?
Hyperkalemic PP is also called potassium-sensitive PP.
What happens to someone with periodic paralysis?
A person with periodic paralysis experiences sudden onset of weakness, which gradually subsides, only to return again later.
How is botulism diagnosed?
Muscle weakness,paralysis,drooping eyelids or a weak voice.
What is the current status of research for periodic paralysis?
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What is a Challenge test for hypokalemic periodic paralysis?
With hypokalemic periodic paralysis an attack of weakness can be induced by administering glucose and insulin with exercise. These tests are potentially hazardous and require careful monitoring.
What is the medical condition periodic paralysis?
Periodic paralysis (PP) is the name for several rare, inherited muscle disorders marked by temporary weakness, especially following rest, sleep, or exercise.
How do you describe periodic paralysis?
Periodic paralysis disorders are genetic disorders that affect muscle strength. There are two major forms, hypokalemic and hyperkalemic, each caused by defects in different genes.
What causes familiar periodic paralysis?
Familiar (genetic) Periodic paralysis comprises a group of rare genetic diseases that cause symptoms such as muscle weakness, muscle stiffness, and complete paralysis. While there more than 30 different strains of periodic paralysis have been identified, the most common include: * Hypokalemic Periodic Paralysis- Caused by reductions in potassium levels, causing the patient to experience weakness and paralysis after eating certain foods or strenuous exercise. * Thyrotoxic Periodic Paralysis- Associated with an overactive thyroid gland. * Hyperkalemic Periodic Paralysis- Weakness, paralysis, and stiffness is experienced after fasting or exercise. * Paramyotonia Congenita- Causes muscle stiffness or weakness as a result of cold temperatures, activity, or low potassium. * Potassium Aggravated Myotonia- Causes muscle stiffness as a result of ingesting potassium. * Malignant Hyperthermia-Caused by a reaction to drugs used in general anaesthetics. While diagnosis of partial paralysis can be extremely difficult, research is offering some new developments. Incidents of partial paralysis can be avoided by staying away from certain hormones, foods, and medications.
What is hyperkalemic periodic paralysis?
The level of potassium in the blood rises slightly or is normal.
What is hypokalemic periodic paralysis?
The level of potassium in the blood falls in the early stages of a paralytic attack.
When did roosevelt develop polio in the national office?
He developed what was diagnosed as infantile paralysis in 1921, before he was elected governor or President.
What is the difference between hypokalemic and hyperkalemic periodic paralysis?
Hypokalemic periodic paralysis is characterized by low levels of potassium in the blood during attacks, leading to muscle weakness or paralysis. In contrast, hyperkalemic periodic paralysis is characterized by high levels of potassium during episodes, resulting in muscle stiffness or weakness. Both conditions are genetic and involve dysfunction in ion channels that regulate potassium levels in muscle cells.
