Cargando…

Predominant Corticospinal Tract Involvement in a Late Infant with Krabbe Disease

A case of late-infantile Krabbe disease in a patient who presented with developmental regression and spastic quadriplegia in late infancy is reported. Brain magnetic resonance imaging (MRI) at 11 months of age showed predominant corticospinal tract involvement, which usually appears in adult Krabbe...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yoshimura, Ayumi, Kibe, Tetsuya, Irahara, Kaori, Sakai, Norio, Yokochi, Kenji
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Libertas Academica 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027888/ https://www.ncbi.nlm.nih.gov/pubmed/27679535 http://dx.doi.org/10.4137/JCM.S40470

Ejemplares similares

Adult Krabbe Disease That Was Successfully Treated with Intravenous Immunoglobulin
por: Fukazawa, Ryosuke, et al.
Publicado: (2020)

Recovery of injured corticospinal tracts after late recanalisation of basilar artery occlusion
por: Li, Xiaodi, et al.
Publicado: (2018)

Low Psychosine in Krabbe Disease with Onset in Late Infancy: A Case Report
por: Corre, Camille S., et al.
Publicado: (2021)

Hepatic Encephalopathy With Corticospinal Tract Involvement Demonstrated by Diffusion Tensor Tractography
por: Bang, Hyun, et al.
Publicado: (2015)

GALC mutations in Chinese patients with late-onset Krabbe disease: a case report
por: Zhuang, Shunzhi, et al.
Publicado: (2019)

Preferential Corticospinal Tract Involvement in a Case of Neuromelioidosis
por: Shanmugam, Sundar, et al.
Publicado: (2021)

Diffusion Tensor Imaging Evaluation of Corticospinal Tract Hyperintensity in Upper Motor Neuron-Predominant ALS Patients
por: Rajagopalan, Venkateswaran, et al.
Publicado: (2011)

Differential involvement of corticospinal tract (CST) fibers in UMN-predominant ALS patients with or without CST hyperintensity: A diffusion tensor tractography study
por: Rajagopalan, Venkateswaran, et al.
Publicado: (2017)

Prion-like α-synuclein pathology in the brain of infants with Krabbe disease
por: Hatton, Christopher, et al.
Publicado: (2022)

Right-left asymmetry in corticospinal tract microstructure and dexterity are uncoupled in late adulthood
por: Demnitz, Naiara, et al.
Publicado: (2021)

Corticospinal Tract and Pontocerebellar Fiber of Central Pontine Myelinolysis
por: Min, Yong, et al.
Publicado: (2012)

Usefulness of dexmedetomidine to prevent emergence agitation in a patient with Krabbe disease: a case report
por: Saito, Junichi, et al.
Publicado: (2018)

Optic nerve enlargement in infantile form of Krabbe disease
por: Castilha-Neto, Dimas, et al.
Publicado: (2012)

Neuroimmune mechanisms in Krabbe's disease
por: Potter, Gregory B., et al.
Publicado: (2016)

Neural tracer for visualization of the corticospinal tract
Publicado: (2012)

Advances in the Diagnosis and Treatment of Krabbe Disease
por: Wenger, David A, et al.
Publicado: (2021)

Compound heterozygous pathogenic variants in the GALC gene cause infant-onset Krabbe disease
por: Zhang, Xiaoli, et al.
Publicado: (2021)

Corticospinal Tract Injury Precedes Thalamic Volume Reduction in Preterm Infants with Cystic Periventricular Leukomalacia
por: Kersbergen, Karina J., et al.
Publicado: (2015)

Diffusion tensor imaging for tracing the corticospinal tract
Publicado: (2012)

Is Corticospinal Tract Degeneration Caused by Sjögren Syndrome?
por: Nam, Tai-Seung, et al.
Publicado: (2018)

Exonic deletions in GALC are frequent in Japanese globoid-cell leukodystrophy patients
por: Irahara-Miyana, Kaori, et al.
Publicado: (2018)

Deterioration of pre-existing hemiparesis due to injury of the ipsilateral anterior corticospinal tract
por: Jang, Sung Ho, et al.
Publicado: (2013)

Does Diffusion Tensor Tractography of the Corticospinal Tract Correctly Reflect Motor Function?
por: Min, Zhi-gang, et al.
Publicado: (2014)

Uncrossed corticospinal tracts in a patient with ichthyosis and hemiparesis: a case report
por: Yang, Huijia, et al.
Publicado: (2020)

Disruption of the Corticospinal Tract in Patients with Acute Lymphoblastic Leukemia: A Case Series
por: Lee, Jae Min, et al.
Publicado: (2022)

Azasugar inhibitors as pharmacological chaperones for Krabbe disease
por: Hill, Chris H., et al.
Publicado: (2015)

Gene therapy for CNS diseases – Krabbe disease
por: Rafi, Mohammad A.
Publicado: (2016)

Krabbe disease: New hope for an old disease
por: Bradbury, Allison M., et al.
Publicado: (2021)

Krabbe disease: A personal perspective and hypothesis
por: Rafi, Mohammad A.
Publicado: (2022)

Neurodegenerative Disorder Risk in Krabbe Disease Carriers
por: Vantaggiato, Lorenza, et al.
Publicado: (2022)

The Effects of Antipsychotics in Experimental Models of Krabbe Disease
por: Sharma, Kapil, et al.
Publicado: (2023)

Globoid Cell Leukodystrophy (Krabbe Disease): An Update
por: Maghazachi, Azzam A
Publicado: (2023)

Neuroradiological, neurophysiological and molecular findings in infantile Krabbe disease: two case reports
por: Vargiami, E, et al.
Publicado: (2016)

Fronto-parietal involvement in chronic stroke motor performance when corticospinal tract integrity is compromised
por: Hordacre, Brenton, et al.
Publicado: (2021)

Motor Evoked Potentials as Potential Biomarkers of Early Atypical Corticospinal Tract Development in Infants with Perinatal Stroke
por: Kowalski, Jesse L., et al.
Publicado: (2019)

Corticospinal tract integrity and motor function following neonatal stroke: a case study
por: Gordon, Anne L, et al.
Publicado: (2012)

Pathologically Proven Gadolinium-enhanced MRI Lesions in the Bilateral Corticospinal Tracts in Lymphomatosis Cerebri
por: Yamaura, Genpei, et al.
Publicado: (2020)

Characteristics of Corticospinal Tract Area According to Pontine Level
por: Seo, Jeong Pyo, et al.
Publicado: (2013)

Structural abnormality of the corticospinal tract in major depressive disorder
por: Sacchet, Matthew D, et al.
Publicado: (2014)

Encoding of forelimb forces by corticospinal tract activity in the rat
por: Guo, Yi, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_7o5aj8si3blc539r4j7fj2hb4n