Search results for "Vertical supranuclear gaze palsy"

showing 4 items of 4 documents

Niemann-Pick disease type C symptomatology: an expert-based clinical description

2013

Niemann-Pick disease type C (NP-C) is a rare, progressive, irreversible disease leading to disabling neurological manifestations and premature death. The estimated disease incidence is 1:120,000 live births, but this likely represents an underestimate, as the disease may be under-diagnosed due to its highly heterogeneous presentation. NP-C is characterised by visceral, neurological and psychiatric manifestations that are not specific to the disease and that can be found in other conditions. The aim of this review is to provide non-specialists with an expert-based, detailed description of NP-C signs and symptoms, including how they present in patients and how they can be assessed. Early dise…

MalePediatricsmedicine.medical_specialtyPsychosisAtaxiaReviewDiseaseGelastic cataplexyDysarthriaDiagnosisMiglustatHumansMedicineGenetics(clinical)Pharmacology (medical)Lysosomal lipid storage diseaseVertical supranuclear gaze palsyCognitive declineGenetics (clinical)DystoniaMedicine(all)Niemann–Pick disease type Cbusiness.industryNiemann-Pick disease type CNiemann-Pick Disease Type CGeneral Medicinemedicine.diseaseDystoniaCognitive impairmentSplenomegalyAtaxiaFemalemedicine.symptombusinessmedicine.drugOrphanet Journal of Rare Diseases
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Neuronal Correlates of Clinical Asymmetry in Progressive Supranuclear Palsy

2014

Progressive supranuclear palsy (PSP) is characterized by a symmetric hypokinetic syndrome with early falls and vertical supranuclear gaze palsy. However, clinically asymmetric manifestations occur, resembling idiopathic Parkinson disease or corticobasal degeneration. The aim of this study was to determine the neuronal correlates of patients suffering from PSP with a lateralized disease manifestation (hemi-PSP) in comparison to patients with symmetric clinical presentation (symPSP) and corticobasal degeneration.Twenty-three patients with PSP and 8 patients with corticobasal degeneration according to standard diagnostic criteria underwent F-fluorodeoxyglucose (FDG) PET scans to assess disease…

Malemedicine.medical_specialtybehavioral disciplines and activitiesBrain mappingProgressive supranuclear palsyPhysical medicine and rehabilitationFluorodeoxyglucose F18mental disordersHumansMedicineCorticobasal degenerationRadiology Nuclear Medicine and imagingAgedAged 80 and overNeuronsBrain MappingVertical supranuclear gaze palsybusiness.industryGeneral MedicinePrognosismedicine.diseaseeye diseasesnervous system diseasesSupranuclear palsyPositron-Emission TomographyFemaleSupranuclear Palsy ProgressivebusinessClinical Nuclear Medicine
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Ocular motor biomarkers in Niemann-Pick disease type C: A prospective cross-sectional multicontinental study in 72 patients

2020

AbstractNiemann-Pick type C (NPC) is a rare lysosomal storage disorder with ocular motor involvement. In a multicontinental, cross-sectional study we characterized ocular motor function in 72 genetically proven patients from twelve countries by means of video-oculography. Interlinking with disease severity, we also searched for ocular motor biomarkers. Our study protocol comprised reflexive and self-paced saccades, smooth pursuit, and gaze-holding in horizontal and vertical planes. Data were compared with those of 158 healthy controls. The Modified Disability Rating Scale, Scale for Assessment and Rating of Ataxia, Spinocerebellar Ataxia Functional Index for neurological status, and Montrea…

medicine.medical_specialtyAtaxiaVertical supranuclear gaze palsyPalsygenetic structuresbusiness.industrymedicine.diseaseSaccadic maskingSmooth pursuitProgressive supranuclear palsyPhysical medicine and rehabilitationSaccademedicineSpinocerebellar ataxiamedicine.symptombusiness
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2021

Introduction Niemann-Pick type C (NPC) is a lysosomal storage disease that is progressive and life-limiting, with an estimated incidence of 1:120,000 live births. In addition to systemic manifestation with (hepato-)splenomegaly, there are a number of neurological manifestations (ataxia, dysarthria, dementia, cataplexy, epileptic seizures, and psychiatric disorders). Characteristic is vertical supranuclear gaze palsy, which is often overlooked. Early diagnosis and start of therapy improve quality of life. This study aimed to characterize oculomotor dysfunction of NPC patients, and to provide ophthalmologic data including retinal imaging. Methods Eighteen patients with biochemically or genet…

medicine.medical_specialtyMultidisciplinaryAtaxiaVertical supranuclear gaze palsyPalsygenetic structuresbusiness.industryRetinalSaccadic maskingchemistry.chemical_compoundmedicine.anatomical_structurechemistryOphthalmologymedicinemedicine.symptomOuter nuclear layerbusinessRetinal thinningOptic discPLOS ONE
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