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1.
Rev. chil. pediatr ; 86(4): 279-282, ago. 2015. graf
Article Dans Espagnol | LILACS | ID: lil-764085

Résumé

Introducción: La rabdomiólisis es una enfermedad poco frecuente en pediatría. El objetivo es presentar un paciente en el que se desarrolló secundario a una deshidratación hipernatrémica grave tras una diarrea aguda. Caso clínico: Lactante de 11 meses que consultó por fiebre, vómitos, diarrea y anuria. Presentó convulsión tónico-clónica autolimitada. Ingresó en mal estado general, severamente deshidratado, con escasa reactividad. En las pruebas complementarias destacó acidosis metabólica grave, hipernatremia e insuficiencia renal prerrenal. Al tercer día apreció leve hipotonía axial y elevación de creatín fosfokinasa 75.076 UI/l, interpretado como rabdomiólisis. Se inició hiperhidratación y alcalinización sistémica, con buena respuesta clínica y bioquímica, siendo dado de alta sin secuelas motoras. Conclusiones: La hipernatremia grave está descrita como causa rara de rabdomiólisis e insuficiencia renal. En pacientes críticos es importante un alto índice de sospecha de rabdomiólisis y determinación seriada de la creatín fosfokinasa para su detección y tratamiento precoz.


Introduction: Rhabdomyolysis is a rare paediatric condition. The case is presented of a patient in whom this developed secondary to severe hypernatraemic dehydration following acute diarrhoea. Case report: Infant 11 months of age who presented with vomiting, fever, diarrhoea and anuria for 15 hours. Parents reported adequate preparation of artificial formula and oral rehydration solution. He was admitted with malaise, severe dehydration signs and symptoms, cyanosis, and low reactivity. The laboratory tests highlighted severe metabolic acidosis, hypernatraemia and pre-renal kidney failure (Sodium [Na] plasma 181 mEq/L, urine density> 1030). He was managed in Intensive Care Unit with gradual clinical and renal function improvement. On the third day, slight axial hypotonia and elevated cell lysis enzymes (creatine phosphokinase 75,076 IU/L) were observed, interpreted as rhabdomyolysis. He was treated with intravenous rehydration up to 1.5 times the basal requirements, and he showed a good clinical and biochemical response, being discharged 12 days after admission without motor sequelae. Conclusions: Severe hypernatraemia is described as a rare cause of rhabdomyolysis and renal failure. In critically ill patients, it is important to have a high index of suspicion for rhabdomyolysis and performing serial determinations of creatine phosphokinase for early detection and treatment.


Sujets)
Animaux , Cochons d'Inde , Lapins , Cytosine/analogues et dérivés , Préparations à action retardée/administration et posologie , Préparations à action retardée/composition chimique , Phosphonates/administration et posologie , Phosphonates/composition chimique , Corps vitré/effets des médicaments et des substances chimiques , Antiviraux/administration et posologie , Antiviraux/composition chimique , Chimie pharmaceutique/méthodes , Cytosine/administration et posologie , Cytosine/composition chimique , Systèmes de délivrance de médicaments/méthodes , Période , Herpès/traitement médicamenteux , Herpèsvirus humain de type 1/effets des médicaments et des substances chimiques , Injections intravitréennes/méthodes , Micelles , Promédicaments/administration et posologie , Promédicaments/composition chimique , Rétine/effets des médicaments et des substances chimiques , Rétine/virologie , Corps vitré/virologie
2.
Indian J Biochem Biophys ; 2001 Feb-Apr; 38(1-2): 1-6
Article Dans Anglais | IMSEAR | ID: sea-26570

Résumé

Methylene blue (MB), an efficient singlet oxygen generating photoactive dye, binds to DNA and allows photosensitized reactions to be used for sequence-specific cleavage of the DNA backbone. Intercalation and groove binding are possible binding modes of the dye, depending on base sequences and environmental conditions. In a recent modeling study of methylene blue binding to a double stranded DNA decamer with an alternating GC sequence, six structural models for intercalation structures and for minor and major groove binding have been obtained. By estimating the binding energies (including electrostatic reaction field contributions of a salt-free aqueous solvent), symmetric intercalation at the 5'-CpG-3' and 5'-GpC-3' steps was found as the predominant binding mode, followed by a slightly weaker binding of the dye in the minor groove. In this study, the stability of the modeled structures has been analysed as a function of salt concentration. The results of finite difference numerical solutions of the non-linear Poisson-Boltzmann equation show that the stabilizing effect of salt is larger for free DNA than for the modeled MB-DNA complexes. Accordingly, the estimated binding energies decrease with increasing ionic strength. A slightly higher stabilization of the groove binding complexes results in comparable binding energies for symmetric intercalation and minor groove binding at high salt concentration. Both results are in qualitative agreement with experimental data.


Sujets)
Ilots CpG , Cytosine/composition chimique , ADN/composition chimique , Antienzymes/pharmacologie , Guanine/composition chimique , Cinétique , Bleu de méthylène/pharmacocinétique , Modèles moléculaires , Modèles statistiques , Conformation d'acide nucléique , Oxygène/métabolisme , Sels/pharmacologie , Thermodynamique
3.
Indian J Biochem Biophys ; 2001 Feb-Apr; 38(1-2): 115-9
Article Dans Anglais | IMSEAR | ID: sea-27945

Résumé

The Crick wobble hypothesis attributes the phenomenon of codon degeneracy to a certain impreciseness of pairing between the third base of the codon and the first base of the anticodon. This theoretical study investigates the pairing properties of some wobble bases, including both, observed and unobserved pairs. Some wobble base-pairs are predicted to follow the Watson-Crick pairs in configuration and pairing facility, while others deviate from this norm. The observed U:V pair is unique in that a pairing configuration may be suggested for it wherein the hydrogen-bonding involves the exocyclic 5-carboxymethoxy group of V. By comparing the theoretical data on the configurations of these pairs with the evidence for their existence/non-existence in nature, some guidelines emerge for differentiating between observed and unobserved base pairs on the basis of the pairing configuration.


Sujets)
Adénine/composition chimique , Anticodon , Appariement de bases , Codon , Simulation numérique , Cytosine/composition chimique , ADN/composition chimique , Guanine/composition chimique , Liaison hydrogène , Inosine/composition chimique , Modèles chimiques , Azote/composition chimique , Conformation d'acide nucléique , Uracile/composition chimique
4.
Indian J Biochem Biophys ; 1995 Dec; 32(6): 429-36
Article Dans Anglais | IMSEAR | ID: sea-26285

Résumé

A GC-rich repetitive sequence (GCRS) of Mycobacterium tuberculosis was identified in our laboratory which displayed a high homology with GC-rich sequences of M. tuberculosis and M. bovis. A PCR assay based on the amplification of the proximal 150 bp of GCRS and its detection by non-radioactive hybridization was developed. The accuracy of the GCRS-based PCR assay was evaluated in a clinical setting for the detection of mycobacterial DNA in pleural fluids for the diagnosis of tuberculosis (TB) using clinical criteria and pleural biopsy histology as gold standard. In a blind study, a total of 67 pleural fluid samples (38 tuberculous and 29 nontuberculous) were analysed by PCR and the results were compared with pleural biopsy, Ziehl-Neelsen staining and culture. Mycobacteria could not be detected by either smear or culture techniques in any of the pleural fluids samples. Out of 38 tuberculous pleural effusions, 24 were positive by PCR (63.2% sensitivity). When PCR results were compared with pleural biopsy histology, an increased sensitivity of 73.3% was obtained. Out of the 29 nontuberculous pleural effusions, 2 false positive results were obtained accounting for an overall specificity of 93.1%. The GCRS-based PCR assay thus has a definite role in the diagnosis of tuberculous pleural effusion in contrast to smear and/or culture techniques.


Sujets)
Séquence d'acides aminés , Séquence nucléotidique , Cytosine/composition chimique , Guanine/composition chimique , Données de séquences moléculaires , Mycobacterium tuberculosis/génétique , Épanchement pleural/diagnostic , Réaction de polymérisation en chaîne , Séquences répétées d'acides nucléiques , Tuberculose pleurale/complications
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