Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0023380 (lethargy)
 5,697 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Two rare clinical manifestations of coenurosis in sheep are reported. (i) A case of partial seizure disorder in a ram of 11 months old. During seizure episodes the animal lay down in lateral recumbency displaying initially a stuporous condition and subsequently began to revolve its head from the base of the cervix. At the necropsy of the case, Coenurus cerebralis cyst (young bladder worm) was found dorsally inside the brainstem, in the site of the tectum mesencephaly. (ii) The second-reported manifestation was a bacterial meningoengephalitis that was witnessed in two lambs of 6-7 weeks old. The lambs displayed lateral recumbency with seizure activity. At necropsy, meningoencephalitis with congestion and abscesses were observed in both of them. Interestingly, C. cerebralis cysts were also found in both brains. Streptococcus dysgalactiae was isolated from the abscesses. Possibly, S. dysgalactiae translocation of the blood-brain barrier was facilitated by the migration of the immature stages of C. cerebralis to and through the brain.
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PMID:Two rare clinical manifestations of coenurosis in sheep. 1702 56

Blood brain barrier disruption enhances drug delivery in primary central nervous system lymphoma. In this study, we report adverse events that were encountered intraoperatively and in the postoperative period in these patients. A retrospective analysis of 17 patients documenting demographic data, preprocedure medical history, intraoperative, and postoperative anesthetic complications was conducted between January 2002 and December 2004. Seventeen patients underwent 210 treatments under general anesthesia with a mean of 12.4+/-7.2 treatments per patient. Focal seizures occurred in 13% of patients. Generalized motor seizures occurred in 4 treatment sessions in 2 different patients. The incidence of seizures was significantly higher when the internal carotid artery was used for injection, as opposed to the vertebral artery (20.8% and 6.02%, respectively, P=0.0034). Tachycardia associated with ST segment depression occurred 9 times (4.3%) in 3 patients. One patient had significant ST segment elevation (more than 1.5 mm). Transient cerebral vasospasm after methotrexate injection occurred in 9% of patients. Postoperative nausea and vomiting were observed in 11.9% of patients. After emergence, lethargy and obtundation occurred in 7.6% of the cases. The incidence of postoperative headache and reversible motor deficits was 6% and 3.8%, respectively. Our review highlights the problems that were encountered during blood brain barrier disruption under anesthesia and in the postoperative period. Further prospective studies are required for comprehensive evaluation of intraprocedure and postprocedure complications that will allow development of an optimal anesthetic plan and will improve patient outcome by preventing potential complications.
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PMID:Perioperative complications of blood brain barrier disruption under general anesthesia: a retrospective review. 1815 25

Menkes disease is an infantile-onset X-linked recessive neurodegenerative disorder caused by diverse mutations in a copper-transport gene, ATP7A. Affected patients are characterized by progressive hypotonia, seizures, failure to thrive and death in early childhood. Here, we report a case of Menkes disease presented by intractable seizures and infantile spasms. A 3-month-old male infant had visited our pediatric clinic for lethargy, floppy muscle tone, poor oral intake and partial seizures. His hair was kinky, brown colored and fragile. Partial seizures became more frequent, generalized and intractable to antiseizure medications. An EEG showed frequent posteriorly dominant generalized spikes that were consistent with a generalized seizure. From a genetic analysis, a c.2743C>T (p.Gln915X) mutation was detected and diagnosed as Menkes disease. The mutation is a novel one that has not been previously reported as a cause of Menkes disease.
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PMID:Identification of a novel mutation in the ATP7A gene in a Korean patient with Menkes disease. 2173 51