| dc.contributor | Martínez Angulo, María Auxiliadora | |
| dc.creator | Zapata Salvatierra, Sofía Galilea | |
| dc.date | 2021-11-10T21:39:00Z | |
| dc.date | 2021-11-10T21:39:00Z | |
| dc.date | 2021 | |
| dc.date.accessioned | 2023-08-08T17:33:20Z | |
| dc.date.available | 2023-08-08T17:33:20Z | |
| dc.identifier | http://dspace.utb.edu.ec/handle/49000/10458 | |
| dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/8052178 | |
| dc.description | Apert syndrome is a genetic anomaly, characterized by the triad of craniosynostosis, syndactyly in the hands and feet, along with a series of dysmorphic features. In the following clinical case, a newborn is diagnosed with Apert syndrome in the neonatology area. An investigation was conducted into Apert syndrome, its causes and complications. An evaluation of the patient, and an evaluation by functional patterns, is performed to be able to perform a nursing care process that is coupled to the patient’s needs. The nursing care process will be carried out using the taxonomies NANDA (diagnostics), NOC (results), NIC (interventions), in order to ensure quality care, and to meet the goals and objectives established in this case study. | |
| dc.description | Apert syndrome is a genetic anomaly, characterized by the triad of craniosynostosis, syndactyly in the hands and feet, along with a series of dysmorphic features. In the following clinical case, a newborn is diagnosed with Apert syndrome in the neonatology area. An investigation was conducted into Apert syndrome, its causes and complications. An evaluation of the patient, and an evaluation by functional patterns, is performed to be able to perform a nursing care process that is coupled to the patient’s needs. The nursing care process will be carried out using the taxonomies NANDA (diagnostics), NOC (results), NIC (interventions), in order to ensure quality care, and to meet the goals and objectives established in this case study. | |
| dc.description | El síndrome de Apert es una anomalía genética, caracterizado por la triada clínica de craneosinostosis, sindactilia en pies y manos, junto con una serie de rasgos dismorficos. En el siguiente caso clínico se presenta a un recién nacido de 72 horas de vida diagnosticada con síndrome de Apert en el Área de neonatología. Se llevó a cabo una investigación sobre el síndrome de Apert, sus causas y complicaciones. Se realiza una valoración a la paciente, y una evaluación por patrones funcionales, para poder realizar un proceso de atención de enfermería que se acople a las necesidades requeridas para su mejoría. El proceso de atención de enfermería se realizara utilizando las taxonomías NANDA (diagnósticos), NOC (resultados), NIC (intervenciones), con el fin de asegurar un cuidado de calidad, y a la par cumplir con las metas y objetivos establecidos en este estudio de caso. | |
| dc.format | 36 p. | |
| dc.format | application/pdf | |
| dc.language | es | |
| dc.publisher | Babahoyo: UTB-FCS, 2021 | |
| dc.rights | Atribución-NoComercial-SinDerivadas 3.0 Ecuador | |
| dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/ec/ | |
| dc.subject | Neonatología | |
| dc.subject | Mutación Genética | |
| dc.subject | Síndrome de Apert | |
| dc.title | Proceso de atención de enfermería en recién nacido con síndrome de Apert | |
| dc.type | bachelorThesis | |
