دورية أكاديمية
Chiari Syndrome: Advances in Epidemiology and Pathogenesis: A Systematic Review
| العنوان: | Chiari Syndrome: Advances in Epidemiology and Pathogenesis: A Systematic Review |
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| المؤلفون: | Rodríguez Blanque, Raquel, Almazán-Soto, Cristina, Piqueras-Sola, Beatriz, SANCHEZ GARCIA, JUAN CARLOS, Reinoso Cobo, Andrés, Menor, María jose |
| المساهمون: | Institut Català de la Salut, Rodríguez-Blanque R Research Group CTS1068, Andalusia Research Plan, Junta de Andalucía, Granada, Spain. San Cecilio University Hospital, Granada, Spain. Nursing Department, Faculty of Health Sciences, University of Granada, Granada, Spain. Almazán-Soto C Vall d’Hebron Hospital Universitari, Barcelona, Spain. Piqueras-Sola B Research Group CTS1068, Andalusia Research Plan, Junta de Andalucía, Granada, Spain. Hospital University Virgen de las Nieves, Granada, Spain. Sánchez-García JC Research Group CTS1068, Andalusia Research Plan, Junta de Andalucía, Granada, Spain. Nursing Department, Faculty of Health Sciences, University of Granada, Granada, Spain. Reinoso-Cobo A Department of Nursing and Podiatry, Faculty of Health Sciences, University of Malaga, Ampliación de Campus de Teatinos, Malaga, Spain. Menor-Rodríguez MJ Área Sanitaria Santiago de Compostela-Barbanza, Subdirección de Humanización y Atención a la Ciudadanía, Santiago de Compostela, Spain, Vall d'Hebron Barcelona Hospital Campus |
| المصدر: | Scientia |
| بيانات النشر: | MDPI |
| سنة النشر: | 2023 |
| مصطلحات موضوعية: | Tub neural - Malformacions, Sistema nerviós - Malalties - Epidemiologia, Fossa cranial posterior - Cirurgia, DISEASES::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Congenital Abnormalities::Nervous System Malformations::Neural Tube Defects::Arnold-Chiari Malformation, ANATOMY::Musculoskeletal System::Skeleton::Bone and Bones::Skull::Skull Base::Cranial Fossa, Posterior, ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Surgical Procedures, Operative::Decompression, Surgical, ENFERMEDADES::enfermedades y anomalías neonatales congénitas y hereditarias::anomalías congénitas::malformaciones del sistema nervioso::defectos del tubo neural::malformación de Arnold-Chiari, ANATOMÍA::sistema musculoesquelético::esqueleto::huesos::cráneo::base del cráneo::fosa craneal posterior, TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::intervenciones quirúrgicas::descompresión quirúrgica |
| الوصف: | Arnold Chiari Syndrome; Hydrocephalus; Scoliosis ; Síndrome de Arnold Chiari; Hidrocefalia; Escoliosis ; Síndrome d'Arnold Chiari; Hidrocefàlia; Escoliosi ; Arnold Chiari syndrome is a rare congenital disease of unknown prevalence and whose origin is still under study. It is encompassed within the posterior cranial malformations, showing a wide spectrum of symptomatology that can range from severe headache, dizziness, and paresthesia to complete asymptomatology. It is for this reason that early diagnosis of the disease is difficult, and it is usually diagnosed in adolescence. Treatment is based on remodeling and decompression of the malformed posterior cranial fossa, although the risk of residual symptoms after surgery is high. The aim of this review is to update all the existing information on this pathology by means of an exhaustive analysis covering all the scientific literature produced in the last 5 years. In addition, it has been carried out following the PRISMA model and registered in PROSPERO with code CRD42023394490. One of the main conclusions based on the results obtained in this review is that the origin of the syndrome could have a genetic basis and that the treatment of choice is the decompression of the posterior cerebral fossa. |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | English |
| تدمد: | 2077-0383 |
| العلاقة: | Journal of Clinical Medicine;12(20); https://doi.org/10.3390/jcm12206694Test; Rodríguez-Blanque R, Almazán-Soto C, Piqueras-Sola B, Sánchez-García JC, Reinoso-Cobo A, Menor-Rodríguez MJ, et al. Chiari Syndrome: Advances in Epidemiology and Pathogenesis: A Systematic Review. J Clin Med. 2023 Oct 23;12(20):6694.; https://hdl.handle.net/11351/10758Test; 001093694200001 |
| DOI: | 10.3390/jcm12206694 |
| الإتاحة: | https://doi.org/10.3390/jcm12206694Test https://hdl.handle.net/11351/10758Test |
| حقوق: | Attribution 4.0 International ; http://creativecommons.org/licenses/by/4.0Test/ ; info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.FB33BDAB |
| قاعدة البيانات: | BASE |
Full Text Finder | تدمد: | 20770383 |
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| DOI: | 10.3390/jcm12206694 |