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  1. Article ; Online: Malformations of the craniocervical junction (chiari type I and syringomyelia

    García-Ramos Rocío / Fernández de Gamboa Fernández de Araoz Marta / Escribano Silva Mercedes / Chesa i Octavio Ester / De la Cruz Labrado Javier / Barrón Fernández Javier / Amado Vázquez María Eugenia / Izquierdo Martínez Maravillas / Isla Guerrero Alberto / Avellaneda Fernández Alfredo / García Ribes Miguel / Gómez Carmen / Insausti Valdivia Joaquín / Navarro Valbuena Ramón / Ramón José R

    BMC Musculoskeletal Disorders, Vol 10, Iss Suppl 1, p S

    classification, diagnosis and treatment)

    2009  Volume 1

    Abstract: Abstract Chiari disease (or malformation) is in general a congenital condition characterized by an anatomic defect of the base of the skull, in which the cerebellum and brain stem herniate through the foramen magnum into the cervical spinal canal. The ... ...

    Abstract Abstract Chiari disease (or malformation) is in general a congenital condition characterized by an anatomic defect of the base of the skull, in which the cerebellum and brain stem herniate through the foramen magnum into the cervical spinal canal. The onset of Chiari syndrome symptoms usually occurs in the second or third decade (age 25 to 45 years). Symptoms may vary between periods of exacerbation and remission. The diagnosis of Chiari type I malformation in patients with or without symptoms is established with neuroimaging techniques. The most effective therapy for patients with Chiari type I malformation/syringomyelia is surgical decompression of the foramen magnum, however there are non-surgical therapy to relieve neurophatic pain: either pharmacological and non-pharmacological. Pharmacological therapy use drugs that act on different components of pain. Non-pharmacological therapies are primarly based on spinal or peripheral electrical stimulation. It is important to determine the needs of the patients in terms of health-care, social, educational, occupational, and relationship issues, in addition to those derived from information aspects, particularly at onset of symptoms. Currently, there is no consensus among the specialists regarding the etiology of the disease or how to approach, monitor, follow-up, and treat the condition. It is necessary that the physicians involved in the care of people with this condition comprehensively approach the management and follow-up of the patients, and that they organize interdisciplinary teams including all the professionals that can help to increase the quality of life of patients.
    Keywords Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Internal medicine ; DOAJ:Medicine (General) ; DOAJ:Health Sciences ; Diseases of the musculoskeletal system ; RC925-935
    Subject code 610
    Language English
    Publishing date 2009-12-01T00:00:00Z
    Publisher BioMed Central
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Malformations of the craniocervical junction (Chiari type I and syringomyelia: classification, diagnosis and treatment).

    Fernández, Alfredo Avellaneda / Guerrero, Alberto Isla / Martínez, Maravillas Izquierdo / Vázquez, María Eugenia Amado / Fernández, Javier Barrón / Chesa i Octavio, Ester / Labrado, Javier De la Cruz / Silva, Mercedes Escribano / de Araoz, Marta Fernández de Gamboa Fernández / García-Ramos, Rocío / Ribes, Miguel García / Gómez, Carmen / Valdivia, Joaquín Insausti / Valbuena, Ramón Navarro / Ramón, José R

    BMC musculoskeletal disorders

    2009  Volume 10 Suppl 1, Page(s) S1

    Abstract: Chiari disease (or malformation) is in general a congenital condition characterized by an anatomic defect of the base of the skull, in which the cerebellum and brain stem herniate through the foramen magnum into the cervical spinal canal. The onset of ... ...

    Abstract Chiari disease (or malformation) is in general a congenital condition characterized by an anatomic defect of the base of the skull, in which the cerebellum and brain stem herniate through the foramen magnum into the cervical spinal canal. The onset of Chiari syndrome symptoms usually occurs in the second or third decade (age 25 to 45 years). Symptoms may vary between periods of exacerbation and remission. The diagnosis of Chiari type I malformation in patients with or without symptoms is established with neuroimaging techniques. The most effective therapy for patients with Chiari type I malformation/syringomyelia is surgical decompression of the foramen magnum, however there are non-surgical therapy to relieve neuropathic pain: either pharmacological and non-pharmacological. Pharmacological therapy use drugs that act on different components of pain. Non-pharmacological therapies are primarily based on spinal or peripheral electrical stimulation. It is important to determine the needs of the patients in terms of health-care, social, educational, occupational, and relationship issues, in addition to those derived from information aspects, particularly at onset of symptoms. Currently, there is no consensus among the specialists regarding the etiology of the disease or how to approach, monitor, follow-up, and treat the condition. It is necessary that the physicians involved in the care of people with this condition comprehensively approach the management and follow-up of the patients, and that they organize interdisciplinary teams including all the professionals that can help to increase the quality of life of patients.
    MeSH term(s) Arnold-Chiari Malformation/classification ; Arnold-Chiari Malformation/complications ; Arnold-Chiari Malformation/diagnosis ; Arnold-Chiari Malformation/psychology ; Arnold-Chiari Malformation/therapy ; Humans ; Syringomyelia/etiology
    Language English
    Publishing date 2009-12-17
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2041355-5
    ISSN 1471-2474 ; 1471-2474
    ISSN (online) 1471-2474
    ISSN 1471-2474
    DOI 10.1186/1471-2474-10-S1-S1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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