Results 1 to 10 of about 1,200 (117)

Adult Reye-like syndrome associated with serologic evidence of acute parvovirus B19 infection [PDF]

Brazilian Journal of Infectious Diseases, 2011
Reye's syndrome is an infrequently diagnosed medical condition affecting mainly children. The etiology, epidemiology and natural history of Reye's syndrome have been cloudily written in footnotes of medical books and exotic papers since the initial ...
Paulo Sérgio Gonçalves da Costa, PhD, Geyza Machado Ribeiro, Thiago Cardoso Vale, Thaís Gomes Casali, Flávio José Barbosa Leite   +4 more
doaj   +6 more sources

Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism [PDF]

BMC Pediatrics, 2002
Background Hyperammonemia, hypoglycemia, hepatopathy, and ventricular tachycardia are common presenting features of carnitine-acylcarnitine translocase deficiency (Mendelian Inheritance in Man database: *212138), a mitochondrial fatty acid oxidation ...
Armstrong Dawna L, Towbin Jeffrey A, Scheuerle Angela E, Scaglia Fernando, Sweetman Lawrence, Wong Lee-Jun C   +5 more
doaj   +2 more sources

REYE-LIKE SYNDROME IN THREE-YEAR-OLD CHILD

Безопасность и риск фармакотерапии, 2018
The article reviews the literature on classical and atypical Reye’s syndrome, explores the circumstances that contribute to its  occurrence, provides criteria for diagnosing with an illustration in the form of an authentic case of Reye-like disease in a ...
S. S. Postnikov, S. V. Mikhailova, G. P. Bryusov, M. N. Kostyleva, A. N. Gratsianskaya, A. E. Ermilin   +5 more
doaj   +3 more sources

Mean platelet volume in children with Reye-like syndrome

Platelets, 2015
Reye-like syndrome (RLS) is considered to be a systemic disorder in which the cytokine storm plays a major role. Mean platelet volume (MPV), which is commonly used as a measure of platelet size, indicates the rate of platelet production and platelet activation. We aimed to study MPV in children with RLS.
Ahmet Sert, Cengizhan Kilicaslan, Sukru Arslan   +2 more
exaly   +3 more sources

A different perspective into clinical symptoms in CPT I deficiency [PDF]

Molecular Genetics and Metabolism Reports
Carnitine palmitoyltransferase I (CPT I) deficiency is an autosomal recessive disorder causing long-chain fatty acid oxidation defect, characterized by metabolic decompensation episodes accompanied by hypoketotic hypoglycemia, hepatomegaly, seizures ...
Mehmet Cihan Balci, Meryem Karaca, Arzu Selamioglu, Huseyin Kutay Korbeyli, Asli Durmus, Belkis Ak, Tugba Kozanoglu, Gulden Fatma Gokcay   +7 more
doaj   +2 more sources

Physiological Perspectives on the Use of Triheptanoin as Anaplerotic Therapy for Long Chain Fatty Acid Oxidation Disorders

Frontiers in Genetics, 2021
Inborn errors of mitochondrial fatty acid oxidation (FAO) comprise the most common group of disorders identified through expanded newborn screening mandated in all 50 states in the United States, affecting 1:10,000 newborns.
Evgenia Sklirou, Ahmad N. Alodaib, Ahmad N. Alodaib, Steven F. Dobrowolski, Al-Walid A. Mohsen, Al-Walid A. Mohsen, Jerry Vockley, Jerry Vockley, Jerry Vockley   +8 more
doaj   +1 more source

Valproic Acid Producing a Reye-Like Syndrome [PDF]

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 1982
SUMMARY:Although several cases of acute hepatic failure associated with the administration of valproic acid (VPA) have been reported, the pathogenesis of this problem remains unclear. We report the case of a 40 month old male with a chronic seizure disorder treated with VPA and phenytoin for two years, who developed sudden progressive neurological ...
D L, Keene, P, Humphreys, B, Carpenter, J P, Fletcher   +3 more
openaire   +2 more sources

Reye Syndrome – A Case Report with Review of Literature .

Journal of Nepal Medical Association, 2008
Here we describe a case of Reye syndrome diagnosed at postmortem liver biopsy of a three-year old girl who presented with vomiting, low grade fever for three days and loss of consciousness for 18 hours.
Arnab Ghosh, S Pradhan, R Swami, S R KC, O P Talwar   +4 more
doaj   +1 more source

Hepatic encephalopathy: An enigma

Muller Journal of Medical Sciences and Research, 2013
Hepatic encephalopathy (HE) is an important and common metabolic disturbance in children. The causes are many. Reye-like syndrome (RLS) can manifest with hypoglycemia, hyperammonemia and altered sensorium with elevated liver enzymes as in Reye syndrome ...
Rajamanickom Saranya, K Shreedhara Avabratha, Aby Dany Varghese, B Sanjeev Rai   +3 more
doaj   +1 more source

Update on Reye Syndrome [PDF]

Journal of Postgraduate Medicine, Education and Research
Reye syndrome, once considered a single clinicopathological entity, is now recognized as an umbrella term encompassing heterogeneous disorders with infectious, metabolic, and toxic etiologies.
Sandeep Negi, Jitendra Kumar Sahu, Pratibha Singhi   +2 more
doaj   +1 more source