Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5.
The present clinical case is based on a 1-year-old female patient 4 months old with a medical diagnosis of CDKL5 deficiency disorder. CDKL5 deficiency is a genetic disorder caused by a pathogenic variant in the CDLK5 gene, which is generally not inherited from any parent, which is linked to the X ch...
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| Formato: | bachelorThesis |
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2022
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| Acceso en línea: | http://dspace.utb.edu.ec/handle/49000/12806 |
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| author | Hurtado Moncayo, Karely Beatriz |
| author_facet | Hurtado Moncayo, Karely Beatriz |
| author_role | author |
| collection | Repositorio Universidad Técnica de Babahoyo |
| dc.contributor.none.fl_str_mv | González García, Walter Adalberto |
| dc.creator.none.fl_str_mv | Hurtado Moncayo, Karely Beatriz |
| dc.date.none.fl_str_mv | 2022-10-14T01:40:30Z 2022-10-14T01:40:30Z 2022 |
| dc.format.none.fl_str_mv | 34 p. application/pdf |
| dc.identifier.none.fl_str_mv | http://dspace.utb.edu.ec/handle/49000/12806 |
| dc.language.none.fl_str_mv | es |
| dc.publisher.none.fl_str_mv | Babahoyo: UTB-FCS, 2022 |
| dc.rights.none.fl_str_mv | Atribución-NoComercial-SinDerivadas 3.0 Ecuador http://creativecommons.org/licenses/by-nc-nd/3.0/ec/ info:eu-repo/semantics/openAccess |
| dc.source.none.fl_str_mv | reponame:Repositorio Universidad Técnica de Babahoyo instname:Universidad Técnica de Babahoyo instacron:UTB |
| dc.subject.none.fl_str_mv | Trastorno CDKL5 Convulsiones Tratamiento dietético |
| dc.title.none.fl_str_mv | Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5. |
| dc.type.none.fl_str_mv | info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/bachelorThesis |
| description | The present clinical case is based on a 1-year-old female patient 4 months old with a medical diagnosis of CDKL5 deficiency disorder. CDKL5 deficiency is a genetic disorder caused by a pathogenic variant in the CDLK5 gene, which is generally not inherited from any parent, which is linked to the X chromosome, which causes serious alterations in neurological development, whose most frequent clinical manifestations are developmental delay, seizures and intellectual disability. The objective of this clinical case is to carry out a nutritional care plan according to their needs and consequently reduce their symptomatology, after obtaining the informed consent of the treatment by the relatives, the nutritional assessment was carried out and the nutritional status of the patient was evaluated, making a comprehensive nutritional diagnosis evidenced by anthropometric values, biochemical, clinical / physical and dietary, it was possible to make a dietary prescription of 1200 kcal / day with 71% fat, 19% carbohydrates and 10% protein (Ketogenic diet) and monitor the evolution of the diet. |
| eu_rights_str_mv | openAccess |
| format | bachelorThesis |
| id | UTB_bdf4ade5ecebc1e9d78533ca5e1f60f6 |
| instacron_str | UTB |
| institution | UTB |
| instname_str | Universidad Técnica de Babahoyo |
| language_invalid_str_mv | es |
| network_acronym_str | UTB |
| network_name_str | Repositorio Universidad Técnica de Babahoyo |
| oai_identifier_str | oai:dspace.utb.edu.ec:49000/12806 |
| publishDate | 2022 |
| publisher.none.fl_str_mv | Babahoyo: UTB-FCS, 2022 |
| reponame_str | Repositorio Universidad Técnica de Babahoyo |
| repository.mail.fl_str_mv | . |
| repository.name.fl_str_mv | Repositorio Universidad Técnica de Babahoyo - Universidad Técnica de Babahoyo |
| repository_id_str | 0 |
| rights_invalid_str_mv | Atribución-NoComercial-SinDerivadas 3.0 Ecuador http://creativecommons.org/licenses/by-nc-nd/3.0/ec/ |
| spelling | Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5.Hurtado Moncayo, Karely BeatrizTrastornoCDKL5ConvulsionesTratamiento dietéticoThe present clinical case is based on a 1-year-old female patient 4 months old with a medical diagnosis of CDKL5 deficiency disorder. CDKL5 deficiency is a genetic disorder caused by a pathogenic variant in the CDLK5 gene, which is generally not inherited from any parent, which is linked to the X chromosome, which causes serious alterations in neurological development, whose most frequent clinical manifestations are developmental delay, seizures and intellectual disability. The objective of this clinical case is to carry out a nutritional care plan according to their needs and consequently reduce their symptomatology, after obtaining the informed consent of the treatment by the relatives, the nutritional assessment was carried out and the nutritional status of the patient was evaluated, making a comprehensive nutritional diagnosis evidenced by anthropometric values, biochemical, clinical / physical and dietary, it was possible to make a dietary prescription of 1200 kcal / day with 71% fat, 19% carbohydrates and 10% protein (Ketogenic diet) and monitor the evolution of the diet.The present clinical case is based on a 1-year-old female patient 4 months old with a medical diagnosis of CDKL5 deficiency disorder. CDKL5 deficiency is a genetic disorder caused by a pathogenic variant in the CDLK5 gene, which is generally not inherited from any parent, which is linked to the X chromosome, which causes serious alterations in neurological development, whose most frequent clinical manifestations are developmental delay, seizures and intellectual disability. The objective of this clinical case is to carry out a nutritional care plan according to their needs and consequently reduce their symptomatology, after obtaining the informed consent of the treatment by the relatives, the nutritional assessment was carried out and the nutritional status of the patient was evaluated, making a comprehensive nutritional diagnosis evidenced by anthropometric values, biochemical, clinical / physical and dietary, it was possible to make a dietary prescription of 1200 kcal / day with 71% fat, 19% carbohydrates and 10% protein (Ketogenic diet) and monitor the evolution of the diet.El presente caso clínico se basa de un paciente femenino de 1 año 4 meses de edad con diagnóstico médico de trastorno por deficiencia de CDKL5. La deficiencia de CDKL5 es un trastorno genético ocasionado por una variante patogénica en el gen CDLK5, que generalmente no hereda de ningún padre, que se encuentra ligado al cromosoma X, el cual, provoca alteraciones graves en el desarrollo neurológico, cuyas manifestaciones clínicas más frecuentes son retraso del desarrollo, convulsiones y discapacidad intelectual. El objetivo de este caso clínico es realizar un plan de atención nutricional de acuerdo a sus necesidades y consecuentemente disminuir su sintomatología, luego de obtener el consentimiento informado del tratamiento por parte de los familiares, se procedió a realizar la valoración nutricional y se concluyó evaluando el estado nutricional del paciente, realizando un diagnóstico integral nutricional evidenciado por valores antropométricos, bioquímicos, clínicos / físicos y dietéticos, se logró realizar una prescripción dietética de 1200 kcal/día con 71%grasa, 19% de carbohidratos y 10% de proteínas (Dieta cetogénica) y monitorear la evolución de la dieta.Babahoyo: UTB-FCS, 2022González García, Walter Adalberto2022-10-14T01:40:30Z2022-10-14T01:40:30Z2022info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/bachelorThesis34 p.application/pdfhttp://dspace.utb.edu.ec/handle/49000/12806esAtribución-NoComercial-SinDerivadas 3.0 Ecuadorhttp://creativecommons.org/licenses/by-nc-nd/3.0/ec/info:eu-repo/semantics/openAccessreponame:Repositorio Universidad Técnica de Babahoyoinstname:Universidad Técnica de Babahoyoinstacron:UTB2022-10-14T08:01:18Zoai:dspace.utb.edu.ec:49000/12806Institucionalhttp://dspace.utb.edu.ec/Universidad públicahttps://utb.edu.ec/http://dspace.utb.edu.ec/oai.Ecuador...opendoar:02026-02-28T22:25:53.231145Repositorio Universidad Técnica de Babahoyo - Universidad Técnica de Babahoyotrue |
| spellingShingle | Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5. Hurtado Moncayo, Karely Beatriz Trastorno CDKL5 Convulsiones Tratamiento dietético |
| status_str | publishedVersion |
| title | Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5. |
| title_full | Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5. |
| title_fullStr | Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5. |
| title_full_unstemmed | Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5. |
| title_short | Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5. |
| title_sort | Proceso de atención nutricional en paciente femenino de 1 año 4 meses de edad con trastorno por deficiencia de CDKL5. |
| topic | Trastorno CDKL5 Convulsiones Tratamiento dietético |
| url | http://dspace.utb.edu.ec/handle/49000/12806 |