Results 71 to 80 of about 4,758 (205)

Atypical myoglobinuria : a new disease ? [PDF]

, 2003
Communication présentée lors des Journées AEEMA-AESA, 22-23 mai 2003National audienceIn autumn 2002 (between 17 October and 31 November), 66 grazing horses (located in 34 french area) suffered a prostrating illness caused by a myopathy and died (56/66 ...
Bernadac, Michel, Bermann, Frédéric, Pitel, Pierre-Hugues, Saison, Anne, Moussu, Claire, Zientara, Stéphan   +5 more
core  

Primary Aldosteronism Presenting as Dropped Head Syndrome With Hypokalemic Rhabdomyolysis: A Case Report

Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.
Background Primary aldosteronism (PA) is a common cause of secondary hypertension and hypokalemia, but it rarely presents with neuromuscular symptoms. Although only a few cases of hypokalemia‐induced rhabdomyolysis have been reported, dropped head syndrome (DHS) due to cervical axial muscle weakness has not previously been described in the context of ...
Ya-Chen Kao, Yu-Cheng Liang, Ye-Fong Du, Horng-Yih Ou, Kalyani Sen   +4 more
wiley   +1 more source

Late and Severe Myopathy in a Patient With Glycogenosis VII Worsened by Cyclosporine and Amiodarone

Frontiers in Neurology, 2019
Glycogenosis VII (GSD VII) is a rare autosomal recessive glycogen storage disorder caused by mutations in the PFKM gene encoding the phosphofructokinase (PFK) enzyme.
Massimiliano Filosto, Stefano Cotti Piccinelli, Anna Pichiecchio, Anna Pichiecchio, Olimpia Musumeci, Anna Galvagni, Filomena Caria, Serena Gallo Cassarino, Enrico Baldelli, Raimondo Vitale, Alessandro Padovani, Antonio Toscano   +11 more
doaj   +1 more source

Exercise induced cramps and myoglobinuria in dystrophinopathy - a report of three Malaysian patients [PDF]

, 2010
Dystrophinopathies commonly present as Duchenne or Becker muscular dystrophy but rare, unusual phenotypes have also been described. We have identified three Malaysian boys with an unusual form of dystrophinopathy, presenting with exercise-induced cramps ...
Annuar, A.A., Alsiddiq, F., Ching, A.S., Wong, S.W., Ong, L.C., Thong, M.K., Goh, K.J., Wong, K.T.   +7 more
core  

Histopathological analysis and in situ localisation of Australian tiger snake venom in two clinically envenomed domestic animals [PDF]

, 2011
Objective: To assess histopathological changes in clinically envenomed tiger snake patients and identify tissue specific localisation of venom toxins using immunohistochemistry.
Jacoby-Alner, T.E., Davern, K.M., Swindells, K., Stephens, N., Balmer, L., Brown, S.G.A.   +5 more
core   +1 more source

Muscle cell membrane damage by very low serum sodium [PDF]

The Pan African Medical Journal, 2009
A 63-year-old male was admitted with complaints of upper gastrointestinal symptoms with fatigue and myalgia. Investigations revealed severe hyponatremia with elevated creatine phosphokinase levels.
Prem Nair, Shine Sadasivan, Vallath Balakrishnan, Joye Varghese, Venkadeswaran Anantha Narayanan   +4 more
doaj  

Rhabdomyolysis and compartment syndrome in a bodybuilder undergoing minimally invasive cardiac surgery

Annals of Cardiac Anaesthesia, 2017
Rhabdomyolysis is the result of skeletal muscle tissue injury and is characterized by elevated creatine kinase levels, muscle pain, and myoglobinuria. It is caused by crush injuries, hyperthermia, drugs, toxins, and abnormal metabolic states.
Sebastian John Baxter, Madhusudan Rao Puchakayala, Vinayak N Bapat   +2 more
doaj   +1 more source

Association between rapid serum sodium correction and rhabdomyolysis in water intoxication: a retrospective cohort study

Journal of Intensive Care, 2017
Background Patients with water intoxication may develop rhabdomyolysis. Existing studies suggest a relationship between the serum sodium correction rate and rhabdomyolysis.
Masahiro Kashiura, Kazuhiro Sugiyama, Yuichi Hamabe   +2 more
doaj   +1 more source

LPIN-1 gene variant in Egyptian children: acute recurrent myoglobinuria

Journal of Rare Diseases
Background Children with LPIN-1 gene variant have recurrent acute myoglobinuria, rose-colored urine, general weakness, and fatigue. Treatment for this gene variant remains ameliorative and supportive. Here, we report the clinical data of three cases from
Tarek M. A. Abdallah, Said S. El-Feky, Nourhan A. A. Salem, Ghada M. Mashaal, Zaghloul E. Gouda   +4 more
doaj   +1 more source

HyperCKemia : Psychosis-Induced Non-Traumatic Rhabdomyolysis [PDF]

, 2021
Rhabdomyolysis is a clinical syndrome that results from skeletal muscle breakdown and the release of intracellular enzymes into systemic circulation. We present a case of transaminitis and serum Creatinine Kinase (CK) levels exceeding 590,000 U/L without
Kim, Eunha, Kramer, Mackenzie, Tzarnas, Stephanie, Rosal, Nathaniel, Chan, Vincent, Butkus, Joann   +5 more
core   +1 more source