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Relevant bibliographies by topics / Arnold Chiari type I malformation

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Academic literature on the topic 'Arnold Chiari type I malformation'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Arnold Chiari type I malformation"

1

Unal, M., and C. Bagdatoglu. "Arnold-Chiari type I malformation presenting as benign paroxysmal positional vertigo in an adult patient." Journal of Laryngology & Otology 121, no. 3 (2006): 296–98. http://dx.doi.org/10.1017/s0022215106003082.

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Arnold-Chiari malformations are a group of congenital hindbrain and spinal cord abnormalities characterized by herniation of the contents of the posterior cranial fossa caudally through the foramen magnum into the upper cervical spine. It is important to recognize Arnold-Chiari type I malformation in the differential diagnosis of adult vertigo cases. We present a 51-year-old patient with Arnold-Chiari type I malformation that was initially diagnosed as posterior semicircular canal benign paroxysmal positional vertigo.

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S.Aithmadouch, K.larbiouassou, A.laaraj, and R.abikassem. "A Case Report on Arnold Chiari Type III: Constellation of Disorders, from Diagnosis to Treatment." Asian Journal of Advanced Research and Reports 18, no. 12 (2024): 297–301. https://doi.org/10.9734/ajarr/2024/v18i12826.

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Arnold-Chiari type III is a malformation characterised by protrusion of the brainstem, cerebellum and lower part of the brain due to a cranial malformation. It is a rare congenital malformation in which the brain protrudes through a fissure in the skull. It occurs during pregnancy when the neural tube of the foetus does not close completely. The Chiari malformation type III, although described in the literature, remains rare, complicating our understanding of their common pathophysiological mechanisms and their management. We report the case of a female infant, admitted for seizure with hypoto

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Nowaczyk, Natalia, and Jolanta Góral-Półrola. "Neuropsychological diagnosis of a female patient with Arnold-Chiari malformation type I." Acta Neuropsychologica 21, no. 4 (2023): 457–78. http://dx.doi.org/10.5604/01.3001.0054.1734.

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Arnold–Chiari I malformation is a congenital malformation of the hindbrain characterized by displacement of the cerebellar tonsils into the foramen magnum, pressure on the fourth ventricle, and decreased fluid flow to the basal cisterns. It is a mild form of the neuro-cranio-vertebral syndrome (Arnold–Chiari syndrome) because in many cases it is asymptomatic or has few clinical signs and symptoms of mild severity.The case study presented in the article concerns a 16.5-year-old patient with Arnold–Chiari I malformation following surgery. Based on the neuropsychological diagnosis, clinical sympt

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Venes, Joan L., Michael A. Di Pietro, and Robert C. Dauser. "Arnold-Chiari Type I Malformation." Contemporary Neurosurgery 10, no. 15 (1988): 6. http://dx.doi.org/10.1097/00029679-198810150-00001.

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Allsopp, G. M., A. Karkanevatos, and R. C. Bickerton. "Abductor vocal fold palsy as a manifestation of type one Arnold Chiari malformation." Journal of Laryngology & Otology 114, no. 3 (2000): 221–23. http://dx.doi.org/10.1258/0022215001905175.

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We report a rare case of type 1 Chiari malformation which presented to the Otolaryngology department with abductor vocal fold palsy following an aspiration pneumonia secondary to absent laryngeal sensation. Chiari malformations and related cases are discussed.

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Voltisa, Lama. "Coexistence of Psychiatric Symptoms and Chiari Type I Malformation - A Case Report." Medicus 1 (October 16, 2018): 35–43. https://doi.org/10.5281/zenodo.7611606.

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Chiari type I malformation has been described infrequently in association with defined psychiatric syndromes. Method: There is a limited literature about obsessions in comorbidity with Chiari malformation. It is described a case of an adolescent with obsessive compulsive disorder and Chiari I malformation and it is reviewed the literature regarding Chiari I malformation and psychiatric disorders. The child came to the attention of child psychiatrist at the age of 7 years old when he manifested developmental delay and various kinds of behavioral symptoms. He was followed up at the age of fiftee

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Teo, Mavis Miqi. "Spinal neuraxial anaesthesia for Caesarean section in a parturient with Type I Arnold–Chiari malformation and syringomyelia." Proceedings of Singapore Healthcare 28, no. 2 (2018): 135–37. http://dx.doi.org/10.1177/2010105818784060.

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Type 1 Arnold–Chiari Malformation is associated with prolapse of the cerebellar tonsils into or below the level of the foramen magnum and is usually diagnosed in adults. There are no current guidelines for the management of patients with a residual Type I Arnold–Chiari Malformation, planned for a Caesarean section under spinal neuraxial anaesthesia. The paucity of literature on this topic presents as a management dilemma. We report a case of a term parturient with Type 1 Arnold–Chiari Malformation, following surgical decompression four years earlier, with a residual syringomyelia who underwent

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Henriques Filho, Paulo Sergio A., and Riccardo Pratesi. "Abnormalities in auditory evoked potentials of 75 patients with Arnold-Chiari malformations types I and II." Arquivos de Neuro-Psiquiatria 64, no. 3a (2006): 619–23. http://dx.doi.org/10.1590/s0004-282x2006000400019.

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OBJECTIVE: To evaluate the frequency and degree of severity of abnormalities in the auditory pathways in patients with Chiari malformations type I and II. METHOD: This is a series-of-case descriptive study in which the possible presence of auditory pathways abnormalities in 75 patients (48 children and 27 adults) with Chiari malformation types I and II were analyzed by means of auditory evoked potentials evaluation. The analysis was based on the determination of intervals among potentials peak values, absolute latency and amplitude ratio among potentials V and I. RESULTS: Among the 75 patients

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George, S., and A. B. Page. "Familial Arnold-Chiari Type I malformation." Eye 20, no. 3 (2005): 400–402. http://dx.doi.org/10.1038/sj.eye.6701887.

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Teo, Miqi Mavis. "Spinal neuraxial anaesthesia for caesarean section in a parturient with type I Arnold Chiari malformation and syringomyelia." SAGE Open Medical Case Reports 6 (January 1, 2018): 2050313X1878611. http://dx.doi.org/10.1177/2050313x18786114.

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Introduction: Type 1 Arnold Chiari malformation is associated with prolapse of the cerebellar tonsils into or below the level of the foramen magnum and is usually diagnosed in adults. There are no current guidelines for the management of patients with a residual type I Arnold Chiari malformation, planned for a caesarean section under spinal neuraxial anaesthesia. The paucity in the literature on this topic presents as a management dilemma. Case report: We report a case of a term parturient with type 1 Arnold Chiari malformation, following surgical decompression 4 years earlier, with a residual

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Dissertations / Theses on the topic "Arnold Chiari type I malformation"

1

Richards, Rachel. "Morphometric-Based Classification For Chiari Malformation Type I." University of Akron / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=akron1438941369.

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NOVELLO, GUY. "L'echographie trans-fontanellaire chez les enfants porteurs d'une myelomeningocele." Limoges, 1988. http://www.theses.fr/1988LIMO0151.

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Shaffer, Nicholas. "A Study of Impedance to Cerebrospinal Fluid Flow in Type I Chiari Malformation." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1301674180.

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Nwotchouang, Blaise Simplice Talla. "SKULL-BASED MORPHOMETRICS AND BRAIN TISSUE DEFORMATION CHARACTERIZATION OF CHIARI MALFORMATION TYPE I." University of Akron / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=akron1595877233083287.

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Shaffer, Nicholas. "Magnetic Resonance Image-Based Hydrodynamic Analysis of Cerebrospinal Fluid Motion in Type I Chiari Malformation." University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1417545898.

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VIDAL, Claudio Henrique Fernandes. "Tratamento cirurgico da malformação de Chiari do tipo I:importância da abertura do forame de Magendie e ressecção das tonsilas." Universidade Federal de Pernambuco, 2014. https://repositorio.ufpe.br/handle/123456789/17973.

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Submitted by Natalia de Souza Gonçalves (natalia.goncalves@ufpe.br) on 2016-10-10T12:57:26Z No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) CLAUDIO VIDAL - COLACAO.pdf: 6023190 bytes, checksum: d165c8659f0d2b209cb4a7a228a33bd7 (MD5)<br>Made available in DSpace on 2016-10-10T12:57:26Z (GMT). No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) CLAUDIO VIDAL - COLACAO.pdf: 6023190 bytes, checksum: d165c8659f0d2b209cb4a7a228a33bd7 (MD5) Previous issue date: 2014-06-13<br>A alta prevalência de malformação da

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Rodrigues, Andre Broggin Dutra. "Marcadores prognósticos em recém-nascidos portadores de mielomeningocele." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/5/5141/tde-20062016-144207/.

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Introdução: Pacientes com mielomeningocele apresentam elevada mortalidade e desenvolvem déficits neurológicos que ocorrem, primariamente, pelo desenvolvimento anormal da medula e de raízes nervosas e, secundariamente, por complicações adquiridas no período pós-natal. O desafio no cuidado desses pacientes é o reconhecimento precoce dos recém-nascidos de risco para evolução desfavorável a fim de estabelecer estratégias terapêuticas individualizadas. Objetivo: Este estudo tem como objetivo identificar marcadores prognósticos de curto prazo para recém-nascidos com mielomeningocele. As característi

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Eppelheimer, Maggie S. "Identification of Chiari Malformation Type I Brain Morphology and Biomechanics: A Multi-Faceted Approach to Determine Diagnostic and Treatment Criteria." University of Akron / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=akron1595680107882868.

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OLIVEIRA, FILHO Marcos Antonio Inacio de. "Cefaleia de esforço em pacientes com má-formação de Chiari tipo I: características anatômicas da fossa posterior e junção crânio-cervical." Universidade Federal de Pernambuco, 2016. https://repositorio.ufpe.br/handle/123456789/18642.

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Submitted by Fabio Sobreira Campos da Costa (fabio.sobreira@ufpe.br) on 2017-04-26T15:31:25Z No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) TESE COMPLETA - MARCOS ANTONIO INACIO DE OLIVEIRA FILHO.pdf: 2169493 bytes, checksum: e337756cb83d4d2819ca9c84d87d318c (MD5)<br>Made available in DSpace on 2017-04-26T15:31:25Z (GMT). No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) TESE COMPLETA - MARCOS ANTONIO INACIO DE OLIVEIRA FILHO.pdf: 2169493 bytes, checksum: e337756cb83d4d2819ca9c84d87d318c (MD5) Previo

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Urbizu, Serrano Aintzane. "Bases genètiques en la malformació de Chiari tipus i." Doctoral thesis, Universitat de Barcelona, 2013. http://hdl.handle.net/10803/145244.

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La malformació de Chiari de tipus I (MCI) s'ha definit tradicionalment com una alteració congènita caracteritzada pel descens de les amígdales cerebel.loses a travès del forat magne en 3 o més mm. Es creu que és conseqüència d'una fosa cranial posterior (FCP) hipoplàstica, amb un os occipital anormalment curt, que resulta d'un mesoderma paraxial insuficient. La simptomatologia descrita pels pacients és molt variada: mals de cap occipitals, cervicàlgies, marejos, vertígens, pèrdua de sensibilitat i de força a les extremitats, alteracions de la son i problemes en la deglució entre d'altres, atri

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Books on the topic "Arnold Chiari type I malformation"

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Anson, John A. Syringomyelia and the Chiari malformations. Edited by AANS Publications Committee. American Association of Neurological Surgeons, 1997.

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Parker, Philip M., and James N. Parker. The official parent's sourcebook on Chiari malformation. ICON Health Publications, 2003.

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F, Chandler William, ed. Ultrasound in neurosurgery. Raven Press, 1990.

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Salman, Michael S. Saccades and saccadic adaptation in children with spina bifida and Arnold-Chiari type II malformation. 2004.

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Tubbs, R. Shane, W. Jerry Oakes, and Mehmet Turgut. Chiari Malformations. Springer International Publishing AG, 2021.

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Tubbs, R. Shane, and W. Jerry Oakes. Chiari Malformations. Springer London, Limited, 2013.

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Tubbs, R. Shane, and W. Jerry Oakes. The Chiari Malformations. Springer, 2013.

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Tubbs, R. Shane, W. Jerry Oakes, and Mehmet Turgut. The Chiari Malformations. Springer, 2020.

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Tubbs, R. Shane, and W. Jerry Oakes. The Chiari Malformations. Springer, 2013.

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Tubbs, R. Shane, and W. Jerry Oakes. The Chiari Malformations. Springer, 2016.

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Book chapters on the topic "Arnold Chiari type I malformation"

1

Maxwell, Megan. "Arnold-Chiari Malformation." In Consults in Obstetric Anesthesiology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-59680-8_13.

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Sarwar, Mohammad. "Arnold-Chiari Malformation." In Computed Tomography of Congenital Brain Malformations. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2571-0_5.

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Liu, Penny P., Penny P. Liu, Gregory D. Arnone, Ashley Kane Palmer, and Raymond F. Sekula. "Surgery for Arnold–Chiari Malformation." In Monitoring the Nervous System for Anesthesiologists and Other Health Care Professionals. Springer US, 2011. http://dx.doi.org/10.1007/978-1-4614-0308-1_25.

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Brock, Roger Schmidt, Mario Augusto Taricco, Matheus Fernandes de Oliveira, Marcelo de Lima Oliveira, Manoel Jacobsen Teixeira, and Edson Bor-Seng-Shu. "Intraoperative Ultrasound in Chiari Type I Malformation." In The Chiari Malformations. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-44862-2_27.

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Thakar, Sumit, Saritha Aryan, Subramaniyan Mani, and R. Raghunatha Sarma. "Predictive Analysis in Chiari Malformation Type I." In The Chiari Malformations. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-44862-2_48.

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Pan, I.-Wen E., and Sandi Lam. "Treatment Costs of Chiari Malformation Type 1." In The Chiari Malformations. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-44862-2_49.

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Beuriat, Pierre-Aurélien, Alexandru Szathmari, Federico Di Rocco, and Carmine Mottolese. "Chiari Type II Malformation: Reversibility Following Myelomeningocele Closure." In The Chiari Malformations. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-44862-2_40.

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Zisakis, Athanasios, Rosa Sun, Joshua Pepper, and Georgios Tsermoulas. "Chiari Malformation Type 1 in Adults." In Advances and Technical Standards in Neurosurgery. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-28202-7_8.

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Massimi, L., F. Novegno, and C. di Rocco. "Chiari type I malformation in children." In Advances and Technical Standards in Neurosurgery. Springer Vienna, 2011. http://dx.doi.org/10.1007/978-3-7091-0673-0_6.

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Liu, Penny P., Chaim I. Nelson, Gregory D. Arnone, Ashley Kane Palmer, and Raymond F. Sekula. "Surgery for Chiari Type I Malformation." In Monitoring the Nervous System for Anesthesiologists and Other Health Care Professionals. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-46542-5_28.

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Conference papers on the topic "Arnold Chiari type I malformation"

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Lacerda, Dhiego Alves de, Pedro Fechine Honorato, Anna Vitória Paz Moreira, et al. "Chiari I malformation: Case report." In IV SEVEN INTERNATIONAL MULTIDISCIPLINARY CONGRESS. Seven Congress, 2024. http://dx.doi.org/10.56238/sevenivmulti2023-159.

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Arnold Chiari type I malformation (CM-I) is a genetic disease first described in 1891 by Hans Chiari (SCHIJMAN, 2004). CM-I is characterized by the descent of the cerebellar tonsils more than 5 mm from the lower margin of the foramen magnum, which can impede the flow of cerebrospinal fluid (CSF) and is often associated with syringomyelia (BALL; CRONE, 1995; ROMERO-LUNA et al., 2022), generating great clinical neurological interest due to the difficulty in diagnosis (MORO et al., 1999).

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Lacerda, Dhiego Alves de, Pedro Fechine Honorato, Anna Vitória Paz Moreira, et al. "Chiari I malformation: Case report." In IV SEVEN INTERNATIONAL MULTIDISCIPLINARY CONGRESS. Seven Congress, 2024. http://dx.doi.org/10.56238/sevenivmulti2023-142.

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Arnold Chiari type I malformation (CM-I) is a genetic disease first described in 1891 by Hans Chiari (SCHIJMAN, 2004). CM-I is characterized by the descent of the cerebellar tonsils more than 5 mm from the lower margin of the foramen magnum, which can impede the flow of cerebrospinal fluid (CSF) and is often associated with syringomyelia (BALL; CRONE, 1995; ROMERO-LUNA et al., 2022), generating great clinical neurological interest due to the difficulty in diagnosis (MORO et al., 1999).

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Demirdogen Cetinoglu, Ezgi, Özge Aydin Guclu, Asli Gorek Dilektasli, Ahmet Ursavas, and Mehmet Karadag. "A case of recurrent pneumonia due to Arnold Chiari malformation." In Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.pa3675.

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Shetty, Deepa, and Harihar Hegde. "Anaesthetic Management of Arnold Chiari Malformation Posted for Foramen Magnum Decompression." In ISACON KARNATAKA 2017 33rd Annual Conference of Indian Society of Anaesthesiologists (ISA), Karnataka State Chapter. Indian Society of Anaesthesiologists (ISA), 2017. http://dx.doi.org/10.18311/isacon-karnataka/2017/ep122.

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Zafar, Adnan, and Nahin Hussain. "peac (cyanotic expiratory apnoea of central origin) in Arnold Chiari II malformation." In ERS/ESRS Sleep and Breathing Conference 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/23120541.sleepandbreathing-2017.p101.

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Rizzatti, F. P. G., and R. P. Amatuzzi. "Late Clinical Presentation of Chiari Malformation Type 1." In American Thoracic Society 2023 International Conference, May 19-24, 2023 - Washington, DC. American Thoracic Society, 2023. http://dx.doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a5855.

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Hernandes Júnior, Paulo Roberto, Juliana de Souza Rosa, Patrick de Abreu Cunha Lopes, et al. "National perspective of the surgical treatment of platibasia and malformation of Arnold Chiari." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.173.

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Background: Platybasia is a bone anomaly, characterized by the flattening of the skull base. Its etiology is still questioned, but it is believed to occur in a congenital way. Objectives: To analyze the panorama of Arnold Chiari’s platelet and malformation surgical treatment procedures in the State of São Paulo and correlate it with the current epidemiology. Methods: observational, descriptive and cross-sectional collection of Arnold Chiari’s platelet and malformation surgical treatment data, available at DATASUS website, from January 2008 up to December 2020 - evaluating the number of hospita

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Hernandes Júnior, Paulo Roberto, Juliana de Souza Rosa, Patrick de Abreu Cunha Lopes, et al. "National perspective of the surgical treatment of platibasia and malformation of Arnold Chiari." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.726.

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Background: Platybasia is a bone anomaly, characterized by the flattening of the skull base. Its etiology is still questioned, but it is believed to occur in a congenital way. Objectives: To analyze the panorama of Arnold Chiari’s platelet and malformation surgical treatment procedures in the State of São Paulo and correlate it with the current epidemiology. Methods: observational, descriptive and cross-sectional collection of Arnold Chiari’s platelet and malformation surgical treatment data, available at DATASUS website, from January 2008 up to December 2020 - evaluating the number of hospita

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Ximenes, Marcelo Tognato, Dan Mohamed Salman, Francisco Tomaz Meneses de Oliveira, and Rubens José Gagliardi. "Downbeat Nystagmus Secondary to Chiari I Malformation." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.374.

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Context: Downbeat nystagmus are characterized by the rapid phase in the down direction in primary position of the eyes, in the most cases represents a cerebellar dysfunction, typically with injuries involving vestibulocerebellum (flocculus, paraflocculus, nodule and uvula), although most cases are due to primary lesions in the brain stem, usually involving paramedian tracts. This type of nystagmus is characteristic of craniocervical abnormalities, such as Chiari 1 malformation, also being seen in a wide variety of cerebellar diseases, including degenerative etiologies, toxic-metabolic and isch

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Cerovac, Anis, Almira Huremović, and Harun Brkić. "Neurosurgical therapy of the Chiari type I malformation with syringomyelia." In NEURI 2015, 5th Student Congress of Neuroscience. Gyrus JournalStudent Society for Neuroscience, School of Medicine, University of Zagreb, 2015. http://dx.doi.org/10.17486/gyr.3.2234.

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Reports on the topic "Arnold Chiari type I malformation"

1

Limbrick, David, Chevis Shannon, Emine Bayman, et al. Comparing Surgery with and without Duraplasty for Youth with Chiari Malformation Type 1 and Syringomyelia. Patient-Centered Outcomes Research Institute® (PCORI), 2024. http://dx.doi.org/10.25302/03.2024.cer.150329700.

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