Results 31 to 40 of about 490,574 (151)

Thyrotoxic hypokalemic periodic paralysis as a rare manifestation of Graves disease

open access: yesВестник хирургии имени И.И. Грекова, 2019
The objectve of the study is to present a rare observation of thyrotoxic hypokalemic periodic paralysis in a Caucasian male. The article presents a clinical observation of 44-year-old man suffering from diffuse toxic goiter. The course of the disease was
A. V. Gostimsky   +4 more
doaj   +1 more source

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   +1 more source

Sjogren's syndrome presenting as hypokalemic periodic paralysis, a rare manifestation: A case series

open access: yesNational Journal of Physiology, Pharmacy and Pharmacology, 2023
Sjogren's syndrome is a chronic and slowly progressing autoimmune disease characterized by lyphocytic infiltration of exocrine glands resulting in Sicca syndrome (xerostomia and keratocunjuntivitis sicca). The disease can present alone or along with
Namita Mohanty   +3 more
doaj   +1 more source

A Case of Thyrotoxic Hypokalemia Periodic Paralysis

open access: yesMedicine Science, 2014
Hypokalemic periodic paralysis is a rare disease characterized by reversible attacks of muscle weakness accompanied by episodic hypokalemia. The most common causes of Hypokalemic periodic paralysis are familial periodic paralysis, thyrotoxic periodic ...
Mazhar Muslum Tuna   +8 more
doaj   +1 more source

THYROTOXIC HYPOKALEMIC PERIODIC PARALYSIS PRESENTING WITH PARAPARESIS

open access: yes, 2013
Thyrotoxic hypokalemic periodic paralysis (THPP) is a rare hyperthyroidism-related endocrine disorder seen predominantly in men of Asian origin. The main characteristics of the disease are hyperthyroidism, hypokalemia, muscle weakness and acute paralysis.
Dogru, Cumali   +4 more
core   +2 more sources

Hypokalemic Thyrotoxic Periodic Paralysis

open access: yesEndocrinology Research and Practice, 2022
Hypokalemia during periodic paralysİs attack was observed in a 22 year old male patient who experienced a total of 3 intermittent paralysis attacks in his extremities.
Hatice Sebile Dökmetaş   +2 more
doaj   +2 more sources

Hypokalemic Periodic Paralysis: Narrative Review

open access: yesВопросы современной педиатрии
Hypokalemic periodic paralysis is a rare genetic pathology characterized by spontaneous muscle weakness up to paralysis along with hypokalemia. The disease development is associated with changes in the CACNA1S, SCN4A, KCNJ2, and KCNJ18 genes regulating ...
Artem A. Ivanov   +2 more
doaj   +1 more source

Recurrent Exertion‐Triggered Transient Bilateral Lower‐Limb Weakness During a Marathon in a Trained Endurance Athlete

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
Running pace profile during the marathon illustrating abrupt reductions in running pace associated with recurrent transient bilateral lower‐limb weakness. ABSTRACT Recurrent, fully reversible bilateral lower‐limb weakness may occur during extreme endurance exercise in the absence of structural spinal or vascular pathology.
Florian Godard
wiley   +1 more source

Surgical treatment for thyrotoxic hypokalemic periodic paralysis: case report

open access: yesWorld Journal of Surgical Oncology, 2012
Thyrotoxic hypokalemic periodic paralysis (THPP) is a rare, potentially life-threatening endocrine emergency. It is characterized by recurrent muscle weakness and hypokalemia.
Lin Yi-Chu   +7 more
doaj   +1 more source

Gene Panel Analysis Reveals Overlapping Genetic Causes of Inherited Cataracts and Other Ocular Phenotypes in Bulgarian Patients

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 7, July 2026.
We have identified 4 pathogenic/likely pathogenic changes and 2 variants of uncertain significance, 3 of which were novel. The identification of disease‐causing variants in the CRYAA, MYH9, RP2, and CLNC1 genes allowed us to establish an accurate genetic diagnosis of inherited cataract and to describe overlapping clinical phenotypes.
Kristiyana Vitanova   +10 more
wiley   +1 more source

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