Hyperkalemic periodic paralysis/Related Articles: Difference between revisions
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==Articles related by keyphrases (Bot populated)== | |||
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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".
Parent topics
Subtopics
Bot-suggested topics
Auto-populated based on Special:WhatLinksHere/Hyperkalemic periodic paralysis. Needs checking by a human.
- 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]