Hyperkalemic periodic paralysis/Related Articles: Difference between revisions
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Latest revision as of 11:01, 30 August 2024
- See also changes related to Hyperkalemic periodic paralysis, or pages that link to Hyperkalemic periodic paralysis or to this page or whose text contains "Hyperkalemic periodic paralysis".
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- Amino acid [r]: Biochemical with an amino group, a carboxyl group, a hydrogen atom, and a side chain bonded to a central carbon. [e]
- Mutation [r]: Changes to the DNA sequence that cause new genetic variation. [e]
- Potassium [r]: A very reactive, silvery white alkali metal, chemical element 19 with symbol K. [e]
- Lymphedema [r]: edema due to obstruction of lymph vessels or disorders of the lymph nodes. [e]
- Autism [r]: Developmental disability that results from a disorder of the human central nervous system. [e]
- Acetylcholine [r]: A chemical transmitter in both the peripheral nervous system (PNS) and central nervous system (CNS) in many organisms including humans. [e]
- Hyperkalaemic periodic paralysis [r]: Genetic disorder, which occurs in humans and horses, characterized by muscle hyperexcitability or weakness which can lead to uncontrolled shaking followed by paralysis. [e]