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1.
Rev. chil. neuro-psiquiatr ; 55(1): 52-63, abr. 2017. tab
Article in Spanish | LILACS | ID: biblio-844482

ABSTRACT

Introduction: Single suture craniosynostosis is the premature closure of one or more cranial sutures. It leads to abnormal skull growth and in some cases to structural and/or functional brain abnormalities. If these anomalies cause a psychomotor development lag and/or cognitive impairment is a controversial topic. This study aims to review the main findings related to psychomotor development and cognitive functioning in children with craniosynostosis, from birth to school age, dividing them into three stages: birth to 3 years, preschool and school. Method: An electronic search was made in PubMed from 2000 to 2015, using the following keywords: "craniosynostosis and neurodevelopment", "craniosynostosis and neuropsychological", "craniosynostosis and cognition". Results: In the early stage of life some children with craniosynostosis can have motor, language and cognition deficits; these impairments are also present in a variable percentage of preschool children, in some cases accompanied with behavior disorders; deficits in attention, executive functions and learning disorders, are reported in school years. Conclusion: Some neuropsychological alterations are found in a variable proportion of patients with craniosynostosis in all stages of development whichare revealed depending on the demands of each age. It is difficult to draw a cognitive profile for this population because of the heterogeneity related to characteristics of the sample, time of assessment, functions assessed and instrument used. It is important to make longitudinal neuropsychological assessments to know how children with craniosynostosis are developing in late stages and to develop consensus about cognitive functions and assessment instruments appropriate for each age.


Introducción: La craneosinostosis simple es el cierre prematuro de una o más suturas craneales que provoca crecimiento anormal del cráneo y en algunos casos anormalidades cerebrales estructurales y/o funcionales. Es un tema controversial si estas anormalidades causan el retraso psicomotor y/o cognitivo reportado en estos pacientes. Esta revisión tiene como objetivo abordar los hallazgos encontrados en el desarrollo psicomotor y cognitivo en niños con craneosinostosis, desde el nacimiento hasta la edad escolar, dividiéndolos en tres etapas: nacimiento a 3 años, etapa preescolar y escolar. Método: Se realizó una búsqueda en PubMed del 2000 al 2015, utilizando estas palabras claves: "craniosynostosis and neurodevelopment", "craniosynostosis and neuropsychological", "Craniosynostosis and cognition". Resultados: En las etapas tempranas de la infancia, los niños con craneosinostosis pueden tener deficiencias motoras, de lenguaje y cognitivas; estos déficits están presentes en un porcentaje variable en la etapa preescolar y pueden acompañarse de alteraciones conductuales; deficiencias atencionales, ejecutivas y de aprendizaje, se reportan en la edad escolar. Conclusión: Se reportan alteraciones neuropsicológicas en un porcentaje variable en estos pacientes en todas las etapas del desarrollo, que se van manifestando conforme las demandas del ambiente. Es difícil establecer un perfil neuropsicológico debido a la heterogeneidad de las características de las muestras en los estudios, el tiempo de la evaluación, las funciones estudiadas y los instrumentos utilizados. Es importante realizar un seguimiento longitudinal para conocer el desarrollo de estos niños, así como el hacer un consenso sobre las funciones cognitivas a evaluar e instrumentos a utilizar para cada edad.


Subject(s)
Humans , Infant, Newborn , Infant , Child, Preschool , Cognition Disorders/epidemiology , Craniosynostoses/epidemiology , Cognition Disorders/etiology , Cognition/physiology , Craniosynostoses/complications , Neuropsychology
3.
Journal of the Korean Ophthalmological Society ; : 1215-1220, 2004.
Article in Korean | WPRIM | ID: wpr-125329

ABSTRACT

PURPOSE: To evaluate the clinical efficacy of a simplified single suture inferior retractor tightening technique in senile entropion. METHODS: Twenty patients (26 eyes) showing no severe horizontal lid laxity underwent an operation for senile entropion between April 2001 and July 2003. After a subciliary incision, the inferior retractor was identified, and repaired by reattaching the superior edge of the inferior retractor to the inferior edge of the lower tarsus using a single 5-0 Prolene suture. RESULTS: The patients were followed up for an average of 2.8 months after surgery. Five patients showed complications: two overcorrections and three recurrences of entropion. The others all showed good cosmetic and functional results. The recurred cases underwent further operation with good results. CONCLUSIONS: The simplified single suture inferior retractor tightening gave good results in patients with senile entropion without severe horizontal lid laxity. Moreover, this procedure has short operation and recovery times. In unilateral cases, more symmetric appearances were obtained compared with combined surgeries.


Subject(s)
Humans , Ankle , Entropion , Polypropylenes , Recurrence , Sutures
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