Results 21 to 30 of about 7,221 (188)

An Instance of Hypokalemic Periodic Paralysis in Adolescent Brothers: A Case Report. [PDF]

open access: yesCureus, 2023
Hypokalemic periodic paralysis (HypoPP) is a rare autosomal dominant disease caused by mutations in either calcium or sodium transmembrane voltage-gated ion channels of skeletal muscle or endoplasmic reticulum.
Calise AC, Carter J, Litvinchuk T.
europepmc   +2 more sources

Case report: SCN4A p.R1135H gene variant in combination with thyrotoxicosis causing hypokalemic periodic paralysis

open access: yesFrontiers in Neurology, 2023
Hypokalemic periodic paralysis (HPP) is a heterogeneous group of diseases characterized by intermittent episodes of delayed paralysis of skeletal muscle with episodes of hypokalemia, caused by variants in CACNA1S or SCN4A genes, or secondary to ...
Zhi Zhang, Banghui Xiao
doaj   +2 more sources

When Potassium Takes a Break: A Case Series of 3 Cases on Hypokalemic Periodic Paralysis. [PDF]

open access: yesClin Case Rep
ABSTRACT This case series highlights three SHPP cases with varied triggers, managed with potassium supplementation and targeted treatments. Early diagnosis, individualized care, and patient education proved vital in preventing recurrence and complications, emphasizing the need for clinical vigilance and tailored approaches in HPP management.
Kaushal Y   +6 more
europepmc   +2 more sources

Physiotherapy Strategies in Hypokalemic Periodic Paralysis: A Case Report. [PDF]

open access: yesCureus
The rare neuromuscular disease known as hypokalemic periodic paralysis (hypoKPP), which results in severe muscle weakness in the extremities, is brought on by abnormalities in potassium transport within cells.
Ambalkar GS   +4 more
europepmc   +2 more sources

“Hashitoxicosis” and possible acquired Gitelman syndrome: dual pathology leading to a catastrophic hypokalemic periodic paralysis

open access: yesAsian Journal of Internal Medicine
Thyrotoxic periodic paralysis (TPP) is more commonly seen in Graves’ disease. But TPP can occur in any condition leading to a hyperthyroid state. It’s important to identify the underlying aetiology of the thyrotoxic state as the management differs with ...
M. S. N. Padmasiri   +4 more
doaj   +2 more sources

SAT507 New Onset Graves’ Thyrotoxicosis Complicated by Hypokalemic Periodic Paralysis: A Late Sequela of COVID- 19 Infection [PDF]

open access: yesJ Endocr Soc, 2023
Disclosure: E. Askar: None. H. Basharat: None. L. Lotfi: None. Y. Jamal: None. Background: Thyrotoxic periodic paralysis (TPP)is a rare endocrine emergency identified by hypokalemia and ascending symmetrical paralysis of extremities.
Esraa Askar   +3 more
europepmc   +2 more sources

Atrial Arrhythmia: A Rare Presentation of Thyrotoxic Hypokalemic Periodic Paralysis

open access: yesIndian Journal of Clinical Cardiology
Thyrotoxic hypokalemic periodic paralysis is a rare but life-threatening complication of hyperthyroidism characterized by hyperthyroidism, hypokalemia, and transient episodes of acute proximal muscle weakness. Incidence of thyrotoxic hypokalemic periodic
Rakesh Chowdary Kotaru   +1 more
doaj   +2 more sources

A Rare Case of Hypokalemic Periodic Paralysis With Acute Urinary Retention: Diagnosis and Management. [PDF]

open access: yesCureus
Hypokalemic periodic paralysis (hypoPP) is a rare channelopathy caused by mutations in skeletal muscle ion channels that usually occurs in young individuals and adolescents.
Sara S, Tv D, Dg G, Elumalai B, Javid M.
europepmc   +2 more sources

Familial hypokalemic periodic paralysis: a case induced by concurrent hyperthyroidism. [PDF]

open access: yesBMC Nephrol
Familial hypokalemic periodic paralysis (HypoPP) is an uncommon genetic disorder characterized by recurrent episodes of muscle weakness and hypokalemia, typically starting in early adulthood.
Hannouneh ZA   +3 more
europepmc   +2 more sources

Hypokalemic Periodic Paralysis Type 2 Due to SCN4A Val1105Met Mutation: A Case Study. [PDF]

open access: yesCureus
Hypokalemic Periodic Paralysis Type 2 (HOKPP2) is a rare autosomal dominant disorder characterized by recurrent episodes of muscle weakness, paralysis, and hypokalemia.
Hu NQ, Yang JY, Lv JL, Zhu YZ, Li LH.
europepmc   +2 more sources

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