نتایج جستجو برای: hypokalemic paralysis

تعداد نتایج: 20271  

2017
A Garza-Alpirez A C Arana-Guajardo J A Esquivel-Valerio M A Villarreal-Alarcón D A Galarza-Delgado

Tubulointerstitial nephritis (TIN) is the main renal involvement associated with primary Sjögren syndrome (pSS). TIN can manifest as distal renal tubular acidosis (RTA), nephrogenic diabetes insipidus, proximal tubular dysfunction, and others. We present a 31-year-old female with hypokalemic paralysis due to distal RTA (dRTA). She received symptomatic treatment and hydroxychloroquine with a goo...

Journal: :Indian pediatrics 1994
V P Dandge W B Pagarkar M Agarwal V R Dharnidharka S P Rathi

Primary hypokalemic periodic paralysis (PHPP) is a rare entity first described by Shakanowitch in 1882. Only a few cases of PHPP have been reported in Indian literature in adults(l). In children hypokalemic paralysis secondary to gastroenteritis and chronic renal disease is much more common than primary disease(2). We hereby report a case of PHPP in a child, successfully managed with acetazolam...

Journal: :Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2006
K Sawanyawisuth S Tiamkao T Pratipanawatr

Myasthenia gravis and hypokalemic periodic paralysis are commonly related with hyperthyroidism but rarely occur together. Here, the authors reported a case of hypokalemic periodic paralysis in a Northeastern Thai woman accompanied with myasthenia gravis. She had motor weakness despite a normal level of serum potassium. Prostigmine test was positive. She dramatically improved after pyridostigmin...

Journal: :International journal of advance research in nursing 2021

Hypokalemic Periodic Paralysis (HypoPP) is a condition that causes episodes of extreme muscle weakness typically beginning in childhood or adolescence. The disorder three to four times more commonly clinically expressed men. Mutations the CACNA1S (calcium voltage-gated channel subunit alpha 1 S) SCN4A (sodium 4) gene can cause Paralysis. primary form genetic and follows an autosomal dominant pa...

Journal: :The Journal of clinical endocrinology and metabolism 2006
Annie W C Kung

CONTEXT The aim of this article was to review the clinical presentation, pathogenesis, and management of thyrotoxic periodic paralysis (TPP). EVIDENCE ACQUISITION A MEDLINE search was conducted for articles published during the last 40 yr based on the key words thyrotoxic periodic paralysis and hypokalemic periodic paralysis. A total of 281 primary articles and 168 references of the retrieved...

Journal: :The Journal of Kartal Training and Research Hospital 2014

Journal: :Journal of the Neurological Sciences 1994

Gholamreza Faridaalaee, Seyed Hesam Rahmani

Hypokalemic periodic paralysis is anautosomal dominantdisease characterized by muscle weakness or paralysis with a matching fall in blood potassium levels. Paralysis attacks often occur in adolescence and are induced by strenuous exercise followed by rest, high carbohydrateor high sodiummeal content, sudden changes in temperature, and even excitement, noise, flashing lights and cold temperature...

Journal: :Journal of the Royal Society of Medicine 1980

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