Search results for "Chiari malformation"

showing 10 items of 15 documents

Clinical and neuroimaging findings in 33 patients with MCAP syndrome: A survey to evaluate relevant endpoints for future clinical trials

2021

Megalencephaly-CApillary malformation-Polymicrogyria (MCAP) syndrome results from somatic mosaic gain-of-function variants in PIK3CA. Main features are macrocephaly, somatic overgrowth, cutaneous vascular malformations, connective tissue dysplasia, neurodevelopmental delay, and brain anomalies. The objectives of this study were to describe the clinical and radiological features of MCAP, to suggest relevant clinical endpoints applicable in future trials of targeted drug therapy. Based on a French collaboration, we collected clinical features of 33 patients (21 females, 12 males, median age of 9.9 years) with MCAP carrying mosaic PIK3CA pathogenic variants. MRI images were reviewed for 21 pat…

AdultMale0301 basic medicinePediatricsmedicine.medical_specialtyCutis marmorataAdolescentClass I Phosphatidylinositol 3-KinasesNeuroimagingContext (language use)Skin Diseases Vascular030105 genetics & heredityCohort StudiesYoung Adult03 medical and health sciencesGeneticsPolymicrogyriamedicineHumansPROSAbnormalities MultipleTelangiectasisMegalencephalyChildMCAP syndromeGenetics (clinical)Chiari malformationClinical Trials as Topicbusiness.industryMacrocephalyPIK3CAmedicine.diseaseMagnetic Resonance ImagingMegalencephaly3. Good healthClinical trial030104 developmental biologyChild PreschoolPostnatal macrocephalyFemalemedicine.symptombusiness[SDV.MHEP]Life Sciences [q-bio]/Human health and pathologyForecastingVentriculomegalyClinical Genetics
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Surgical Treatment in Symptomatic Chiari Malformation Type I: A Series of 25 Adult Patients Treated with Cerebellar Tonsil Shrinkage

2019

Background: The variety of symptoms and radiological findings in patients with Chiari malformation type I makes both the indication for surgery and the technical modality controversial. We report our 5-year experience, describing our technique and critically evaluating the clinical results. Methods: Between 2012 and 2016, 25 patients (15 female and 10 male; mean age 39.2 years) underwent posterior fossa decompression for Chiari malformation type I. Their clinical complaints included headache, nuchalgia, upper limb weakness or numbness, instability, dizziness and diplopia. Syringomyelia was present in 12 patients (48%). Suboccipital craniectomy was completed in all cases with C1 laminectomy …

AdultMaleDecompressive Craniectomymedicine.medical_specialtyCerebellar Vermi030218 nuclear medicine & medical imaging03 medical and health sciencesChiari malformation type I0302 clinical medicineCHIARI MALFORMATION TYPE IElectrocoagulationmedicineDuraplastyIn patientSurgical treatmentCerebellar tonsil shrinkageAdult patientsSettore MED/27 - Neurochirurgiabusiness.industryLaminectomyDecompression Surgicalmedicine.diseaseMagnetic Resonance ImagingSyringomyeliaArnold-Chiari MalformationSurgeryPosterior fossa decompressionTreatment Outcomemedicine.anatomical_structureRadiological weaponCerebellar tonsilFemalebusiness030217 neurology & neurosurgerySyringomyeliaHuman
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Assessment of brainstem function in Chiari II malformation utilizing brainstem auditory evoked potentials (BAEP), blink reflex and masseter reflex

2000

Brainstem dysfunction was evaluated in 67 patients with myelomeningocele and Chiari II malformation using brainstem auditory evoked potentials (BAEP), blink reflex (BR) and masseter reflex (MR). Signs and symptoms related to Chiari II malformation were observed in 18 patients while 49 patients had normal brainstem findings. BAEP and BR showed a higher sensitivity of brainstem involvement than MR (BAEP=1.0, BR=0.83, MR=0.50). BR, and in particular, MR were of higher accuracy (BR=0.52, MR=0.72) than BAEP (0.39) in separating patients with brainstem signs and symptoms related to Chiari II malformation. We feel that this is due to anatomic and physiologic peculiarities of the brainstem structur…

AdultMaleMeningomyeloceleAdolescentgenetic structuresCentral nervous systemSigns and symptomsSensitivity and SpecificityCentral nervous system diseaseDevelopmental NeuroscienceReflexEvoked Potentials Auditory Brain Stemotorhinolaryngologic diseasesmedicineHumansCorneal reflexChildBlinkingMasseter Musclebusiness.industryGeneral Medicinemedicine.diseaseArnold-Chiari Malformationmedicine.anatomical_structureChild PreschoolAnesthesiaPediatrics Perinatology and Child HealthReflexFemaleNeurology (clinical)BrainstembusinessJaw jerk reflexNormal brainstemBrain StemHydrocephalusBrain and Development
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Monosymptomatic presentation of type I Arnold-Chiari malformation: report of two cases.

1994

Two cases of type I ACM are described, one of which presented with dizziness in late childhood (case 1), the other with mild intention tremor in adulthood (case 2). Cerebellar ectopia should be considered in monosymptomatic patients even in the absence of other symptoms and signs of C.N.S. dysfunction. Magnetic resonance imaging of the craniocervical junction should be performed because it may be diagnostic for type I ACM.

AdultMalePediatricsmedicine.medical_specialtyNeurologyAdolescentDermatologytype I Arnold-Chiari malformationCerebellummedicineType I Arnold Chiari MalformationHumansNeuroradiologycerebellar tonsils ectopiamedicine.diagnostic_testbusiness.industryGeneral NeuroscienceBrainMagnetic resonance imagingGeneral MedicineCraniocervical junctionMagnetic Resonance ImagingSurgeryArnold-Chiari MalformationPsychiatry and Mental healthSettore MED/26 - NeurologiaIntention tremorFemaleNeurology (clinical)NeurosurgeryPresentation (obstetrics)medicine.symptombusinessItalian journal of neurological sciences
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Brainstem evoked potentials and magnetic resonance imaging abnormalities in differential diagnosis of intracranial hypotension.

2019

Summary Objective To compare brainstem acoustic evoked potentials (BAEP) and magnetic resonance imaging (MRI) in the differential diagnosis of intracranial hypotension (IH), Chiari malformation (CM) and sensorineural hearing loss (SNHL). Methods BAEP were recorded in 18 IH, 18 CM, 20 SNHL patients and 52 controls. MRI were acquired in all IH and CM patients. Results Abnormal BAEP were observed in 94% of IH patients, in 33% of CM and 70% of SNHL patients. After recovery from IH, BAEP abnormalities disappeared. Internal auditory canal (IAC) MRI abnormalities were described in 88% of IH patients. MRI signs of IH were observed in 33–78% in IH patients, but the most frequent MRI sign was 8th ner…

AdultMalegenetic structuresHearing Loss SensorineuralChiari malformationIntracranial HypotensionSensitivity and Specificity050105 experimental psychologyDiagnosis Differential03 medical and health sciences0302 clinical medicinePhysiology (medical)otorhinolaryngologic diseasesmedicineEvoked Potentials Auditory Brain StemHumans0501 psychology and cognitive sciencesIn patientIntracranial HypotensionChiari malformationmedicine.diagnostic_testbusiness.industry05 social sciencesBrainMagnetic resonance imagingGeneral MedicineMiddle Agedmedicine.diseaseMagnetic Resonance ImagingHyperintensityArnold-Chiari MalformationSensorineural hearing lossNeurologyBrainstem acoustic evoked potentialSensorineural hearing lossSettore MED/26 - NeurologiaFemaleNeurology (clinical)BrainstemDifferential diagnosisNuclear medicinebusiness030217 neurology & neurosurgeryNeurophysiologie clinique = Clinical neurophysiology
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Masseter reflex and blink reflex abnormalities in Chiari II malformation.

2001

Masseter reflex and blink reflex were evaluated in 64 patients with a myelomeningocele and Chiari II malformation. In 46 patients, no brainstem signs or symptoms were present. Brainstem dysfunction related to Chiari II malformation occurred in 18 patients. The masseter reflex was more frequently abnormal in the symptomatic than asymptomatic patients (P = 0.02). Although the blink reflex was similarly affected in the two groups of patients (P > 0.1), it was very sensitive, being abnormal in 83% of symptomatic and 65% of asymptomatic patients. Concomitant abnormality of masseter reflex and the late contralateral blink reflex component (R2c) was almost exclusively found in symptomatic patients…

AdultMalemedicine.medical_specialtyMeningomyeloceleAdolescentPhysiologyAsymptomaticSensitivity and SpecificityCentral nervous system diseaseCellular and Molecular NeurosciencePhysiology (medical)medicineHumansCorneal reflexChildChi-Square DistributionBlinkingMasseter MuscleElectrodiagnosismedicine.diseaseElectric StimulationSurgeryArnold-Chiari MalformationAnesthesiaConcomitantCiliospinal reflexChild PreschoolFemaleNeurology (clinical)Brainstemmedicine.symptomAbnormalityPsychologyJaw jerk reflexMusclenerve
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Quality of Life in Individuals Affected by Arnold Chiari Malformation: Comparison and Validation of a Measurement Instrument.

2017

BACKGROUND Introduction. Arnold Chiari Malformation (ACM) type I is a pathology whose symptomatology has repercussions for the quality of life of those affected by it. Quality-of-life measurement instruments can allow the severity of the impact of Chiari type I malformation on patients' lives to be monitored. The Chiari Symptom Profile (CSP) is a valid and reliable instrument designed for this purpose. The aim of the study was to adapt the CSP to Spanish and to explore the reliability and validity of this construct in the context of Spanish-speaking patients with ACM. METHODS The English CSP instrument has a good internal validity and consistency. We used a standardized procedure for the li…

AdultMalemedicine.medical_specialtyPsychometricsEndocrinology Diabetes and MetabolismHealth StatusContext (language use)Linguistic validation030218 nuclear medicine & medical imagingCorrelation03 medical and health sciences0302 clinical medicineQuality of lifeCronbach's alphaCost of IllnessPredictive Value of TestsSickness Impact ProfileSurveys and QuestionnairesImmunology and AllergyMedicineHumansInternal validityReliability (statistics)business.industryfungiReproducibility of ResultsMiddle AgedTranslatingSyringomyeliaArnold-Chiari MalformationSpainScale (social sciences)Physical therapyQuality of LifeFemalebusiness030217 neurology & neurosurgeryEndocrine, metabolicimmune disorders drug targets
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Somatosensory evoked potentials in Arnold-Chiari malformation.

2002

Abstract Nearly all patients with repaired myelomeningoceles have an Arnold–Chiari (AC) malformation and about 20% of these patients develop clinical signs of brainstem dysfunction. The management of symptomatic AC malformation is still controversial and techniques are needed to provide an objective assessment of brainstem function. We recorded somatosensory evoked potentials (SEPs) in 52 patients aged between 8 months and 20 years (median 7.3 years) with AC malformation, to determine whether the SEPs discriminate patients with symptomatic AC malformation from those without symptoms. The subcortical far-field components P13, P14 and N18, which are generated within the brainstem, were record…

AdultYounger ageMeningomyeloceleAdolescentNeural ConductionSigns and symptomsLate onsetSomatosensory systemSensitivity and SpecificityDevelopmental NeurosciencePredictive Value of TestsEvoked Potentials SomatosensoryMedicineHumansIn patientChildbusiness.industryInfantReproducibility of ResultsGeneral MedicineArnold-Chiari MalformationSpinal CordSomatosensory evoked potentialAnesthesiaChild PreschoolPediatrics Perinatology and Child HealthNeurology (clinical)BrainstemArnold chiaribusinessBrain StemBraindevelopment
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Megalencephaly Syndromes and Activating Mutations in the PI3K-AKT Pathway: MPPH and MCAP

2013

The megalencephaly‐polymicrogyria‐polydactyly‐hydrocephalus (MPPH) and megalencephaly‐capillary malformation (MCAP) syndromes are highly recognizable and partly overlapping disorders of brain overgrowth (megalencephaly). Both syndromes are characterized by congenital or early postnatal megalencephaly, with a high risk for progressive ventriculomegaly leading to hydrocephalus and cerebellar tonsillar ectopia leading to Chiari malformation, and cortical brain abnormalities, specifically polymicrogyria. MCAP is further characterized by distinct cutaneous capillary malformations, finger or toe syndactyly, postaxial polydactyly, variable connective tissue dysplasia and mild focal or segmental bo…

GeneticsPathologymedicine.medical_specialtyThymomaBiologymedicine.diseaseAKT3GermlineGermline mutationGeneticsPolymicrogyriamedicineMegalencephalyGenetics (clinical)PI3K/AKT/mTOR pathwayChiari malformationAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics
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Exophthalmos and basilar impression. A contribution to differential diagnosis of endocrine orbitopathy.

1988

We report on a male patient with exophthalmos of unclear etiology, basilar impression, syringohydromyelia and type II Arnold-Chiari malformation. Two diseases involving the orbital region were to be considered in differential diagnostic terms: endocrine orbitopathy and osseous orbit dysplasia. The typical physical appearance associated with basilar impression as well as suppurative keratitis in Lagophthalmos was striking. Tetraspasticity with pareses, bulbar symptoms, proximally pronounced muscular atrophy as well as a left hemihypesthesia was shown neurologically. Although the orbit CT was normal, sonography revealed thickened ocular muscles. There was euthyroidism in diffuse goiter with n…

MalePathologymedicine.medical_specialtyExophthalmosLagophthalmosContext (language use)Endocrine System DiseasesVascular anomalyAutoimmune DiseasesDiagnosis DifferentialAtrophyPlatybasiamedicineOrbital DiseasesExophthalmosHumansbusiness.industryGeneral MedicineMiddle Agedmedicine.diseaseeye diseasesSyringomyeliaArnold-Chiari Malformationmedicine.anatomical_structureDysplasiaSurgerysense organsNeurology (clinical)Differential diagnosismedicine.symptombusinessTomography X-Ray ComputedOrbit (anatomy)Neurosurgical review
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