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1.
J Pediatr Orthop B ; 16(4): 273-80, 2007 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-17527106

RESUMEN

The treatment of infantile Blount's disease remains controversial. The progressive development of epiphysiodesis of the medial tibial physis induced a complex deformity of the lower limb such as severe genu varum, joint incongruity, torsion instability and leg length discrepancy with major functional consequences. Nine knees on eight children (average age was 7 years and 2 months) were treated by a one-time procedure using a specific external fixator that combined elevation of the medial tibial plateau, axial correction in the valgus, complete sterilization of the upper tibial growth cartilage, leg lengthening anticipation and de-rotation if necessary. Magnetic resonance imaging was useful to describe the deformity and to prepare for surgery. Corrections were progressively obtained through the physis plan by means of short incisions and the use of a specific external fixator. The primary results at an average of 24 months were good with a low rate of complications but final evaluation will be conducted at the end of the children's growth period.


Asunto(s)
Enfermedades del Desarrollo Óseo/cirugía , Fijadores Externos , Osteogénesis por Distracción/métodos , Tibia/anomalías , Tibia/cirugía , Niño , Diseño de Equipo , Femenino , Humanos , Inestabilidad de la Articulación/cirugía , Articulación de la Rodilla/cirugía , Diferencia de Longitud de las Piernas/etiología , Diferencia de Longitud de las Piernas/cirugía , Imagen por Resonancia Magnética , Masculino , Cuidados Preoperatorios , Tibia/patología , Resultado del Tratamiento
2.
BMC Med Genomics ; 9: 6, 2016 Jan 22.
Artículo en Inglés | MEDLINE | ID: mdl-26801768

RESUMEN

BACKGROUND: Necrotizing enterocolitis (NEC) is the most frequent life-threatening gastrointestinal disease experienced by premature infants in neonatal intensive care units. The challenge for neonatologists is to detect early clinical manifestations of NEC. One strategy would be to identify specific markers that could be used as early diagnostic tools to identify preterm infants most at risk of developing NEC or in the event of a diagnostic dilemma of suspected disease. As a first step in this direction, we sought to determine the specific gene expression profile of NEC. METHODS: Deep sequencing (RNA-Seq) was used to establish the gene expression profiles in ileal samples obtained from preterm infants diagnosed with NEC and non-NEC conditions. Data were analyzed with Ingenuity Pathway Analysis and ToppCluster softwares. RESULTS: Data analysis indicated that the most significant functional pathways over-represented in NEC neonates were associated with immune functions, such as altered T and B cell signaling, B cell development, and the role of pattern recognition receptors for bacteria and viruses. Among the genes that were strongly modulated in neonates with NEC, we observed a significant degree of similarity when compared with those reported in Crohn's disease, a chronic inflammatory bowel disease. CONCLUSIONS: Gene expression profile analysis revealed a predominantly altered immune response in the intestine of NEC neonates. Moreover, comparative analysis between NEC and Crohn's disease gene expression repertoires revealed a surprisingly high degree of similarity between these two conditions suggesting a new avenue for identifying NEC biomarkers.


Asunto(s)
Enfermedad de Crohn/complicaciones , Enfermedad de Crohn/genética , Enterocolitis Necrotizante/complicaciones , Enterocolitis Necrotizante/genética , Perfilación de la Expresión Génica , Transducción de Señal/genética , Antivirales/metabolismo , Femenino , Humanos , Inmunidad Innata/genética , Recién Nacido , Masculino , Embarazo , Reproducibilidad de los Resultados , Análisis de Secuencia de ARN
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