Results 51 to 60 of about 1,029 (132)
Core myopathy in two siblings with a biallelic variant in the CACNA1S gene—A case series study
Clinical Case Reports, Volume 12, Issue 8, August 2024.Key Clinical Message Homozygous variants of Calcium Voltage‐Gated Channel Subunit Alpha1 S (CACNA1S) gene mutation were previously identified as causes of periodic paralysis and congenital early‐onset myopathy, while it could be manifested as a late‐onset congenital core myopathy.
Tara Khoeini +7 more
wiley +1 more source
Annals of Indian Academy of Neurology, 2012 Objective: There is paucity of reports on thyrotoxic periodic paralysis (TPP) from India. We report the patients with TPP and compare them with idiopathic hypokalemic periodic paralysis (IHPP).
J Kalita +4 more
doaj +1 more source
Periodic Paralysis: A Case Series with a Literature Review
Case Reports in NeurologyIntroduction: Periodic paralysis is a condition that causes recurrent episodes of flaccid paralysis, and it can be primary or secondary. Hypokalemic periodic paralysis is the most common type of primary periodic paralysis, and it is inherited through ...
Bassem Al Hariri +5 more
doaj +1 more source
Thyrotoxic periodic paralysis in an adolescent male: A case report and literature review
Clinical Case Reports, 2021 Thyrotoxic periodic paralysis (TPP) is rarely seen in children and adolescents. Clinical manifestations in children and adolescents may vary. It is important for clinicians to be aware of this rare and life‐threatening condition.
Luke He +3 more
doaj +1 more source
Paralisia periódica tireotóxica.
Acta Médica Portuguesa, 2005 Thyrotoxic periodic paralysis (TPP) is characterized by recurrent episodes of muscle weakness and hypokalemia associated with thyroid hyperactivity. Reported predominantly among individuals of Asian descent, TPP is a rare manifestation of hyperthyroidism
José Vale +3 more
doaj +1 more source
Airway Management of Hypokalaemic Paralysis with Trismus and Bulbar Palsy Due To Conn's Syndrome
The Laryngoscope, Volume 135, Issue 6, Page 2070-2072, June 2025.
Cristian Aragón‐Benedí +3 more
wiley +1 more source
Thyrotoxic Hypokalemic Periodic Paralysis Triggered by Dexamethasone Administration
Acta Medica, 2020 Thyrotoxic hypokalemic periodic paralysis (THPP) is a disease characterized by recurrent episodes of muscle weakness due to intracellular potassium shifting in the presence of high levels of thyroid hormone.
Waraporn Polamaung +4 more
doaj +1 more source
Paralisia periódica tireotóxica.
Acta Médica Portuguesa, 2012 Thyrotoxic periodic paralysis (TPP) is characterized by recurrent episodes of muscle weakness and hypokalemia associated with thyroid hyperactivity. Reported predominantly among individuals of Asian descent, TPP is a rare manifestation of hyperthyroidism
José Vale +3 more
doaj +1 more source
Doenças musculares no hipertiroidismo.
Acta Médica Portuguesa, 1995 Hyperthyroidism may present various muscular diseases, namely thyrotoxic chronic myopathy, myasthenia gravis, disthyroid ophthalmopathy and thyrotoxic periodic paralysis.
F Pissarra +5 more
doaj +1 more source
Thyrotoxic Hypokalemic Periodic Paralysis: A Case Report
Endocrinology Research and Practice, 2012 Thyrotoxic hypokalemic periodic paralysis is a rare complication of thyrotoxicosis. This clinic condition is often encountered in Asian populations and male gender while thyrotoxicosis is frequently seen in women. The escape of potassium into cell is the
Murat Atmaca +4 more
doaj +1 more source