Periodic Paralysis in Young People in an African Setting: Two Unexpected Causes in Cameroon
Paralysie Périodique Chez le Jeune en Milieu Africain : Deux Étiologies Inattendues au Cameroun
DOI:
https://doi.org/10.5281/zenodo.19635825Keywords:
Periodic paralysis, CACNA1S gene mutation, Thyrotoxicosis, CameroonAbstract
Periodic paralysis in young individuals is a rare neuromuscular disorder characterized by recurrent episodes of muscle weakness that resolve spontaneously or following appropriate treatment. We report two cases of periodic paralysis in young patients presenting with similar clinical features. The clinical picture was dominated by quadriplegia associated with hypokalemia. The underlying causes were a mutation of the CACNA1S gene in the first patient and Graves' disease in the second. The outcome was favorable after correction of hypokalemia in the first case and after appropriate management of hyperthyroidism in the second, with complete resolution of paralytic episodes. These two cases highlight the importance of considering periodic paralysis in any presentation of acute flaccid paralysis in the Black African population, particularly in young male patients.
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Copyright (c) 2026 Hassana Samir, Hadja Inna Astasselbe, Fouwou Njoya Charifa, Sidi Cedric Tchameni, Abdoul Aziz, Hamadou Bâ

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