Search results for "onset."

showing 10 items of 478 documents

Commentary: Anderson‐Fabry Disease: A Rare Cause of Levodopa‐Responsive Early Onset Parkinsonism

2021

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Pediatricsmedicine.medical_specialtyLevodopaAnderson-Fabry DiseaseNeurologybusiness.industrymedicineAnderson-Fabry disease early onset parkinsonism levodopa response lysosomal storage diseasesNeurology (clinical)Early onset parkinsonismbusinessCase Reports and Commentariesmedicine.drugMovement Disorders Clinical Practice
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Migraine in Children Under 7 Years of Age: a Review

2020

Purpose of review: Despite the accumulation of a significant amount of data on pediatric headache, few studies have been conducted on its occurrence in children under 7 years of age. Within primary headaches in this age, migraine especially, turns out to be a disorder affecting up to 4% of the general population. An underestimate of its true prevalence can be due to lack of specific diagnostic markers, the frequent difficulty of describing pain in childhood, and the necessity of reliable parents’ reports. Thus, migraine in children under 7 years of age represents an important challenge for clinicians. The objective of this manuscript is to provide a comprehensive review of epidemiologic, cl…

Pediatricsmedicine.medical_specialtyMigraine DisordersPain medicinePopulation03 medical and health sciences0302 clinical medicinePrimary headacheRisk Factors030202 anesthesiologyHumansMedicineAge of OnsetChildeducationChildrenMigraineEmbryo-fetal developmenteducation.field_of_studyPreschoolersbusiness.industryAge FactorsBrainGeneral MedicinePediatric headachemedicine.diseasePediatric headacheNatural historyAnesthesiology and Pain MedicineMigraineChild PreschoolAnticipation (genetics)Neurology (clinical)business030217 neurology & neurosurgeryPediatric populationCurrent Pain and Headache Reports
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Age at symptom onset, diagnosis, and enzyme replacement therapy (ERT) initiation among family members with mucopolysaccharidosis II (Hunter Syndrome)…

2013

Pediatricsmedicine.medical_specialtyMucopolysaccharidosis IIbusiness.industryEndocrinology Diabetes and MetabolismHunter syndromeEnzyme replacement therapymedicine.diseaseBiochemistrySurgeryEndocrinologyGeneticsmedicineSymptom onsetbusinessMolecular BiologyMolecular Genetics and Metabolism
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An international, phase 3, switchover study of reveglucosidase alfa (BMN 701) in subjects with late-onset Pompe disease

2015

Pediatricsmedicine.medical_specialtyNeurologybusiness.industryPediatrics Perinatology and Child HealthSwitchoverMedicineLate onsetNeurology (clinical)DiseasebusinessGenetics (clinical)SurgeryNeuromuscular Disorders
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1035 The International Registry for Niemann-Pick Disease Type C (NP-C) in Clinical Practice

2012

Background and Aim An international disease registry was started in September 2009 to evaluate the long-term disease course of NP-C in clinical settings. Methods Descriptive data from enrolment are presented for all patients with available data who were included in the Registry as of 19 th August 2011. Results 121 patients have been enrolled. The median (range) age at enrolment was 16.9 (0.9−56.6) years, age at onset of neurological manifestations was 8.2 ( Conclusions Over two-thirds of this NP-C cohort had infantile or juvenile onset of neurological manifestations; neonatal jaundice was observed more frequently in these patients versus adolescent/adult-onset patients.

Pediatricsmedicine.medical_specialtyNiemann–Pick disease type Cbusiness.industryClinical settingsJaundicemedicine.diseaseDisease courseClinical PracticeJuvenile onsetDisease registryPediatrics Perinatology and Child HealthCohortmedicinemedicine.symptombusinessArchives of Disease in Childhood
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Therapy Strategies for Usher Syndrome Type 1C in the Retina

2014

The Usher syndrome (USH) is the most common form of inherited deaf-blindness with a prevalence of ~ 1/6,000. Three clinical subtypes (USH1–USH3) are defined according to the severity of the hearing impairment, the presence or absence of vestibular dysfunction and the age of onset of retinitis pigmentosa (RP). USH1 is the most severe subtype with congenital severe to profound hearing loss and onset of RP before puberty. Currently only the amelioration of the hearing deficiency is implemented, but no treatment of the senso-neuronal degeneration in the eye exists.

Pediatricsmedicine.medical_specialtyRetinabusiness.industryUsher syndromemacromolecular substancesDegeneration (medical)medicine.diseaseProfound hearing lossmedicine.anatomical_structurenervous systemRetinitis pigmentosaotorhinolaryngologic diseasesmedicineDeaf blindnessVestibular dysfunctionAge of onsetbusiness
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Late-Onset Sarcoidosis in a 77-Year-Old Man

2015

International audience

Pediatricsmedicine.medical_specialtySarcoidosisbusiness.industry[SDV.MHEP.GEG]Life Sciences [q-bio]/Human health and pathology/Geriatry and gerontologymedicineLate onsetSarcoidosis[ SDV.MHEP.GEG ] Life Sciences [q-bio]/Human health and pathology/Geriatry and gerontologyGeriatrics and Gerontologymedicine.diseasebusinessComputingMilieux_MISCELLANEOUS
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Clinical Presentation of Patients with Adult Late-Onset Telomere Biology Disorders - Results from the Aachen Telomeropathy Registry

2021

Abstract Introduction: Telomere biology disorders (TBD) are caused by mutations affecting proper telomere maintenance resulting in premature telomere shortening. Telomere length (TL) assessment is currently being used for screening and diagnosis of TBD of which Dyskeratosis congenita (DKC) is the most prominent TBD subtype typically found in children and adolescents. In adults, TBDs are characterized by a broad spectrum of more "cryptic" diverging mono- or oligosymptomatic clinical manifestations such as bone marrow failure (BMF), hepatopathy or interstitial lung disease (ILD). However, despite growing general clinical awareness and exertion of improved TL screening strategies, insufficient…

Pediatricsmedicine.medical_specialtyTelomere biologybusiness.industryImmunologymedicineLate onsetCell BiologyHematologyPresentation (obstetrics)businessBiochemistryBlood
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Early Referral to an ALS Center Reduces Several Months the Diagnostic Delay: A Multicenter-Based Study.

2020

Objective: To analyze those factors contributing to the diagnostic delay in ALS.Methods: Consecutive ALS patients were categorized as those studied in departmental hospitals and those studied in a referral ALS center. Demographic and clinical variables, together with data of the diagnostic pathway were collected. Multivariable models were used to assess their effect in the time between symptoms onset and the first neurologist visit (time symptoms-neurologist), in the time between the first neurologist visit and the diagnosis (time neurologist-diagnosis) and in the diagnostic delay.Results: 166 ALS patients with a median diagnostic delay of 11.53 months (IQR: 6.68, 15.23) were included. The …

Pediatricsmedicine.medical_specialtyamyotrophic lateral sclerosisALS UnitClinical variablesReferrallcsh:RC346-42903 medical and health sciences0302 clinical medicinemental disordersmedicine030212 general & internal medicineAmyotrophic lateral sclerosislcsh:Neurology. Diseases of the nervous systemOriginal Researchdiagnostic timelinesbusiness.industryUpper motor neuronmedicine.diseasediagnostic delaynervous system diseasesdiagnostic pathwaymedicine.anatomical_structureNeurologyReferral centerBulbar onsetProgression rateNeurology (clinical)business030217 neurology & neurosurgeryEarly referralFrontiers in neurology
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Early psychosis in Thauvin‐Robinet‐Faivre syndrome, a complication of the disease?

2021

Pediatricsmedicine.medical_specialtybusiness.industryEarly psychosisDiseasePhenotypePsychotic DisordersGeneticsmedicineHumansAbnormalities MultipleGenetic Predisposition to DiseaseDisease SusceptibilityAge of OnsetComplicationbusinessGenetic Association StudiesGenetics (clinical)Clinical Genetics
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