RÉSUMÉ
BACKGROUND: Spontaneous cerebellar hemorrhage (CH) is a critical neurosurgical event. It is usually categorized as a homogenous group under the general term of deep/nonlobar intracerebral hemorrhage. However, increasing evidence suggests it is composed of 2 subgroups, separated from each other by their anatomic location (deep vs. superficial), as well as by their vascular etiology (small vessel disease vs. cerebral amyloid angiopathy). OBJECTIVE: To identify any clinically significant differences between anatomically separated subgroups of CHs: deep versus superficial. METHODS: This is a retrospective study on patients who were diagnosed with spontaneous CHs at a single tertiary center. On the basis of the radiologic location of the hematoma, patients were divided into 2 groups: deep (group 1) and superficial (group 2). Computerized medical records were extracted for multiple variables. RESULTS: A total of 69 patients fulfilled the inclusion criteria. Fifty-three (77%) were in group 1, and 16 (23%) were in group 2. Having any vascular risk factor was associated with the highest odds ratio for having a deep CH. Morbid obesity (body mass index ≥30) and the use of antiplatelets were also associated with increased odds ratios. Group 1 is also associated with high prevalence of intraventricular hemorrhage, acute hydrocephalus, and less favorable outcome. CONCLUSIONS: This study supports the notion that CH is most likely a heterogenous condition, composed of 2 subgroups, separated from each other in terms of anatomic location, vascular etiologies, and clinical consequences. Further studies on large cohort of patients are needed in order to accurately define the subgroups of this life-threatening event.
Sujet(s)
Maladies du cervelet/étiologie , Maladies du cervelet/anatomopathologie , Hémorragie cérébrale/étiologie , Hémorragie cérébrale/anatomopathologie , Adulte , Sujet âgé , Maladies du cervelet/classification , Hémorragie cérébrale/classification , Femelle , Humains , Mâle , Adulte d'âge moyen , Études rétrospectives , Facteurs de risqueRÉSUMÉ
Cerebellar tonsil herniation comprises a spectrum of disorders sharing a common neuroimaging finding consisting of downward displacement of the cerebellar tonsils through the foramen magnum and into the upper cervical spinal canal. This not uncommon condition may result from a large host of congenital or acquired causes, and confusion regarding its classification and pathogenesis still exists. Terminology also remains heterogeneous, including inconsistencies in the usage of the "Chiari 1" monicker. In this paper, the hypothesized mechanisms of development of tonsillar herniation are reviewed and strategies of management are discussed, with particular attention to surgical options adapted to the underlying etiology. A focus will be placed on acquired causes of tonsillar herniation.
Sujet(s)
Malformation d'Arnold-Chiari/classification , Malformation d'Arnold-Chiari/chirurgie , Maladies du cervelet/classification , Maladies du cervelet/chirurgie , Hernie/classification , Hernie/thérapie , Malformation d'Arnold-Chiari/imagerie diagnostique , Maladies du cervelet/imagerie diagnostique , Hernie/imagerie diagnostique , Humains , Imagerie par résonance magnétique , Procédures de neurochirurgie/méthodesRÉSUMÉ
BACKGROUND: A revised classification of cerebellar infarctions (CI) may uncover unrecognized associations with etiologic stroke subtypes. We hypothesized that obliquely oriented small cortical cerebellar infarction (SCCI) representing end zone infarctions on MRI would be associated with cardiac embolism. METHODS: We retrospectively analyzed consecutive stroke patients recruited between January-December 2016 in our center. Analyzed baseline characteristics: sex, age, cardiovascular risk factors, history of stroke or atrial fibrillation (AF). TOAST classification was used for determining stroke subtype. Acute infarction location (anterior/posterior/mixed anterior-posterior circulation), acute uni- or multiterritorial infarction, and acute or chronic CI/SCCI/non-SCCI were assessed by MRI, and vertebrobasilar stenosis/occlusion by vessel imaging. Pre-specified analysis was also performed in patients without known high cardioembolic risk (known AF history or acute multiterritorial infarction). RESULTS: We included 452 patients (CI in 154, isolated SCCI in 55, isolated non-SCCI in 50, and mixed SCCI/non-SCCI in 49). Both SCCI and non-SCCI were associated with AF history (SCCI, p = 0.021; non-SCCI, p = 0.004), additional acute posterior circulation infarction (p < 0.001 both CI-subtypes), multiterritorial infarctions (SCCI, p = 0.003; non-SCCI, p < 0.001) and cardioembolic more frequent than large-artery atherosclerosis origin (p < 0.001 for both CI-subtypes). SCCI was associated with older age (p < 0.001), whereas non-SCCI was associated with stroke history (p = 0.036) and vertebrobasilar stenosis/occlusion (p = 0.002). SCCI were older (p = 0.046) than non-SCCI patients, had less frequently prior stroke (p < 0.001), and more frequent cardioembolic infarction (p = 0.025). In patients without known high cardioembolic risk (n = 348), SCCI was strongly associated with subsequent cardioembolism diagnosis (OR 3.00 [CI 1.58-5.73, p < 0.001]). No such association was present in non-SCCI. CONCLUSIONS: Acute or chronic SCCI are strongly associated with a cardioembolic origin.
Sujet(s)
Fibrillation auriculaire/complications , Infarctus encéphalique/étiologie , Maladies du cervelet/étiologie , Embolie intracrânienne/étiologie , Accident vasculaire cérébral/étiologie , Sujet âgé , Sujet âgé de 80 ans ou plus , Infarctus encéphalique/classification , Infarctus encéphalique/anatomopathologie , Maladies du cervelet/classification , Maladies du cervelet/anatomopathologie , Femelle , Humains , Embolie intracrânienne/classification , Embolie intracrânienne/anatomopathologie , Mâle , Adulte d'âge moyen , Études rétrospectives , Facteurs de risque , Accident vasculaire cérébral/classification , Accident vasculaire cérébral/anatomopathologieRÉSUMÉ
BACKGROUND & OBJECTIVE: Non-invasive brain stimulation (NIBS) might be a valuable therapeutic approach for neurological diseases by modifying the cortical activity in the human brain and promoting neural plasticity. Currently, researchers are exploring the use of NIBS on the cerebellum to promote functional neural changes in cerebellar disorders. In the presence of cerebellar dysfunction, several movement disorders, such as kinetic tremor, ataxia of gait, limb dysmetria and oculomotor deficits, become progressively more disabling in daily life, and no pharmacological treatments currently exist. CONCLUSION: In the present mini-review, we report the main evidence concerning the use of NIBS in three specific cerebellar dysfunctions, cerebellar ataxias (CA), essential tremor (ET) and ataxic cerebral palsy, in which abnormalities of neuroplasticity and cortical excitability can be important pathophysiological factors.
Sujet(s)
Maladies du cervelet/thérapie , Cervelet/physiologie , Stimulation cérébrale profonde/méthodes , Animaux , Maladies du cervelet/classification , HumainsSujet(s)
Maladies du cervelet/diagnostic , Angle pontocérébelleux/anatomopathologie , Imagerie par résonance magnétique , Tumeurs du système nerveux périphérique/anatomopathologie , Maladies du cervelet/classification , Angle pontocérébelleux/anatomie et histologie , Angle pontocérébelleux/imagerie diagnostique , Nerfs crâniens/anatomopathologie , Humains , Neurinome de l'acoustique/anatomopathologie , Neurinome de l'acoustique/physiopathologie , Tumeurs du système nerveux périphérique/complications , TomodensitométrieRÉSUMÉ
Pontocerebellar hypoplasia (PCH) is a clinically and genetically heterogeneous group of autosomal recessively inherited neurodevelopmental disorders. Following the rapidly increasing number of genes identified in different subtypes, the clinical spectrum has been broadened to completely different neurological phenotypes. In this review we will address the clinical picture, neuroradiological, pathoanatomic, and genetic findings in the currently known PCH subtypes.
Sujet(s)
Maladies du cervelet/classification , Maladies du cervelet/génétique , Maladies du cervelet/anatomopathologie , Cervelet/physiopathologie , Diagnostic différentiel , Humains , Imagerie par résonance magnétique , Neuroimagerie , PhénotypeRÉSUMÉ
Previous findings suggested that the human cerebellum is involved in the acquisition but not the long-term storage of motor associations. The finding of preserved retention in cerebellar patients was fundamentally different from animal studies which show that both acquisition and retention depends on the integrity of the cerebellum. The present study investigated whether retention had been preserved because critical regions of the cerebellum were spared. Visual threat eye-blink responses, that is, the anticipatory closure of the eyes to visual threats, have previously been found to be naturally acquired conditioned responses. Because acquisition is known to take place in very early childhood, visual threat eye-blink responses can be used to test retention in patients with adult onset cerebellar disease. Visual threat eye-blink responses were tested in 19 adult patients with cerebellar degeneration, 27 adult patients with focal cerebellar lesions due to stroke, 24 age-matched control subjects, and 31 younger control subjects. High-resolution structural magnetic resonance images were acquired in patients to perform lesion-symptom mapping. Voxel-based morphometry was performed in patients with cerebellar degeneration, and voxel-based lesion-symptom mapping in patients with focal disease. Visual threat eye-blink responses were found to be significantly reduced in patients with cerebellar degeneration. Visual threat eye-blink responses were also reduced in patients with focal disease, but to a lesser extent. Visual threat eye-blink responses declined with age. In patients with cerebellar degeneration the degree of cerebellar atrophy was positively correlated with the reduction of conditioned responses. Voxel-based morphometry showed that two main regions within the superior and inferior parts of the posterior cerebellar cortex contributed to expression of visual threat eye-blink responses bilaterally. Involvement of the more inferior parts of the posterior lobe was further supported by voxel-based lesion symptom mapping in focal cerebellar patients. The present findings show that the human cerebellar cortex is involved in long-term storage of learned responses.
Sujet(s)
Maladies du cervelet/complications , Conditionnement palpébral/physiologie , Incapacités d'apprentissage/étiologie , Dégénérescence nerveuse/complications , Adulte , Sujet âgé , Cartographie cérébrale , Études cas-témoins , Maladies du cervelet/classification , Maladies du cervelet/étiologie , Femelle , Latéralité fonctionnelle , Humains , Traitement d'image par ordinateur , Modèles linéaires , Imagerie par résonance magnétique , Mâle , Adulte d'âge moyen , Dégénérescence nerveuse/étiologie , Stimulation lumineuse , Temps de réaction/physiologie , /physiologie , Indice de gravité de la maladie , Statistique non paramétrique , Accident vasculaire cérébral/étiologieRÉSUMÉ
Recent research indicates that physiotherapy can improve motor performance of patients with cerebellar degeneration. Given the known contributions of the cerebellum to motor learning, it remains unclear whether such observable changes in performance are mediated by the cerebellum or cerebral brain areas involved in motor control and learning. The current study addressed this question by assessing the increase in gray matter volume due to sensorimotor training in cerebellar patients using voxel-based morphometry. Nineteen human subjects with pure cerebellar degeneration and matched healthy controls were trained for 2 weeks on a balance task. Postural and clinical assessments along with structural magnetic resonance imaging were performed pretraining and post-training. The main findings were as follows. First, training enhanced balance performance in cerebellar patients. Second, in contrast to controls patients revealed significantly more post-training gray matter volume in the dorsal premotor cortex. Third, training-related increase in gray matter volume was observed within the cerebellum and was more pronounced in controls than in patients. However, statistically cerebellar changes were at the trend level and thus require additional, independent confirmation. We conclude that sensorimotor training of patients with cerebellar neurodegeneration induces gray matter changes primarily within nonaffected neocortical regions of the cerebellar-cortical loop. Residual function of the cerebellum appears to be exploited suggesting either a recovery from degeneration or intact processes of cerebellar plasticity in the remaining healthy tissue.
Sujet(s)
Encéphale/physiopathologie , Maladies du cervelet/rééducation et réadaptation , Traitement par les exercices physiques/méthodes , Plasticité neuronale/physiologie , Posture/physiologie , Adulte , Sujet âgé , Analyse de variance , Encéphale/anatomopathologie , Maladies du cervelet/classification , Maladies du cervelet/anatomopathologie , Évaluation de l'invalidité , Femelle , Études de suivi , Humains , Traitement d'image par ordinateur , Imagerie par résonance magnétique , Mâle , Adulte d'âge moyen , Activité motrice , Effort physique , Performance psychomotrice/physiologie , Résultat thérapeutiqueRÉSUMÉ
Oral-Facial-Digital Syndrome type VI (OFD VI) represents a rare phenotypic subtype of Joubert syndrome and related disorders (JSRD). In the original report polydactyly, oral findings, intellectual disability, and absence of the cerebellar vermis at post-mortem characterized the syndrome. Subsequently, the molar tooth sign (MTS) has been found in patients with OFD VI, prompting the inclusion of OFD VI in JSRD. We studied the clinical, neurodevelopmental, neuroimaging, and genetic findings in a cohort of 16 patients with OFD VI. We derived the following inclusion criteria from the literature: 1) MTS and one oral finding and polydactyly, or 2) MTS and more than one typical oral finding. The OFD VI neuroimaging pattern was found to be more severe than in other JSRD subgroups and includes severe hypoplasia of the cerebellar vermis, hypoplastic and dysplastic cerebellar hemispheres, marked enlargement of the posterior fossa, increased retrocerebellar collection of cerebrospinal fluid, abnormal brainstem, and frequently supratentorial abnormalities that occasionally include characteristic hypothalamic hamartomas. Additionally, two new JSRD neuroimaging findings (ascending superior cerebellar peduncles and fused thalami) have been identified. Tongue hamartomas, additional frenula, upper lip notch, and mesoaxial polydactyly are specific findings in OFD VI, while cleft lip/palate and other types of polydactyly of hands and feet are not specific. Involvement of other organs may include ocular findings, particularly colobomas. The majority of the patients have absent motor development and profound cognitive impairment. In OFD VI, normal cognitive functions are possible, but exceptional. Sequencing of known JSRD genes in most patients failed to detect pathogenetic mutations, therefore the genetic basis of OFD VI remains unknown. Compared with other JSRD subgroups, the neurological findings and impairment of motor development and cognitive functions in OFD VI are significantly worse, suggesting a correlation with the more severe neuroimaging findings. Based on the literature and this study we suggest as diagnostic criteria for OFD VI: MTS and one or more of the following: 1) tongue hamartoma(s) and/or additional frenula and/or upper lip notch; 2) mesoaxial polydactyly of one or more hands or feet; 3) hypothalamic hamartoma.
Sujet(s)
Imagerie par résonance magnétique/méthodes , Neuroimagerie/méthodes , Syndromes oro-facio-digitaux/diagnostic , Syndromes oro-facio-digitaux/anatomopathologie , Malformations multiples/diagnostic , Malformations multiples/anatomopathologie , Adolescent , Adulte , Maladies du cervelet/classification , Maladies du cervelet/diagnostic , Maladies du cervelet/génétique , Maladies du cervelet/anatomopathologie , Cervelet/malformations , Enfant , Enfant d'âge préscolaire , Malformations oculaires/classification , Malformations oculaires/diagnostic , Malformations oculaires/génétique , Malformations oculaires/anatomopathologie , Femelle , Humains , Nourrisson , Nouveau-né , Maladies kystiques rénales/classification , Maladies kystiques rénales/diagnostic , Maladies kystiques rénales/génétique , Maladies kystiques rénales/anatomopathologie , Mâle , Syndromes oro-facio-digitaux/classification , Syndromes oro-facio-digitaux/génétique , Phénotype , Polydactylie/diagnostic , Polydactylie/anatomopathologie , Rétine/malformations , Rétine/anatomopathologie , Jeune adulteRÉSUMÉ
The influence of the cerebellum on independent finger control has rarely been investigated. We examined multidigit control in 22 patients with cerebellar degeneration, 20 patients with cerebellar stroke, and 21 patients with surgical lesions after cerebellar tumor removal. In the first task, either the index finger or the middle finger was actively lifted from an object during static holding. Both controls and cerebellar patients increased the forces of the nearby digits in synchrony with lift-off to maintain the total finger force. Patients used increased finger forces but showed no significant deficits in the pattern and timing of rearrangement of finger forces. In the second task, subjects had to press and release one finger against a force-sensitive keypad with the other fingers being inactive. All patient groups showed increased force production of the noninstructed (enslaved) fingers compared with controls. Lesion-symptom mapping in the focal patients revealed that lesions of the superior hand area were related to abnormal levels of enslaving. Increased finger forces in the finger-lifting task likely reflect an unspecific safety strategy. Increased effects of enslaving in the individuated key-press task, however, may be explained by a deterioration of cerebellar contribution to feedforward commands necessary to suppress activity in noninstructed fingers or by increased spread of the motor command intended for the instructed finger. Despite the large and diverse patient sample, surprisingly few abnormalities were observed. Both holding an object and finger typing are overlearned, automatized motor tasks, which may not or little depend on the integrity of the cerebellum.
Sujet(s)
Maladies du cervelet/complications , Doigts/physiopathologie , Troubles des habiletés motrices/étiologie , Mouvement/physiologie , Performance psychomotrice/physiologie , Adolescent , Adulte , Sujet âgé , Analyse de variance , Phénomènes biomécaniques , Maladies du cervelet/classification , Maladies du cervelet/anatomopathologie , Cervelet/anatomopathologie , Doigts/innervation , Latéralité fonctionnelle , Force de la main/physiologie , Humains , Traitement d'image par ordinateur , Imagerie par résonance magnétique , Mâle , Adulte d'âge moyen , Jeune adulteRÉSUMÉ
A group of disorders with disparate symptomatology, including congenital cerebellar ataxia, retinal blindness, liver fibrosis, polycystic kidney disease, and polydactyly, have recently been united under a single disease mechanism called 'ciliopathies'. The ciliopathies are due to defects of the cellular antenna known as the primary cilium, a microtubule-based extension of cellular membranes found in nearly all cell types. Key among these ciliopathies is Joubert syndrome, displaying ataxia, oculomotor apraxia, and mental retardation* with a pathognomonic 'molar tooth sign' on brain magnetic resonance imaging. The importance of ciliary function in neuronal development has been appreciated only in the last decade with the classification of Joubert syndrome as a ciliopathy. This, together with the identification of many of the clinical features of ciliopathies in individuals with Joubert syndrome and the localization of Joubert syndrome's causative gene products at or near the primary cilium, have defined a new class of neurological disease. Cilia are involved in diverse cellular processes including protein trafficking, photoreception, embryonic axis patterning, and cell cycle regulation. Ciliary dysfunction can affect a single tissue or manifest as multi-organ involvement. Ciliary defects have been described in retinopathies such as retinitis pigmentosa and Leber congenital amaurosis (defects in photoreceptor ciliary protein complexes), renal syndromes with nephronophthisis and cystic dysplastic kidneys, and liver conditions such as fibrosis and biliary cirrhosis. Recognizing the diverse presentations of the ciliopathies and screening strategies following diagnosis is an important part of the treatment plan of children with cilia-related disorders.
Sujet(s)
Maladies du cervelet/complications , Maladies du cervelet/anatomopathologie , Cils vibratiles/anatomopathologie , Apraxies/congénital , Syndrome de Bardet-Biedl , Maladies du cervelet/classification , Troubles de la motilité ciliaire , Syndrome de Cogan , Malformations oculaires , Humains , Amaurose congénitale de Leber , Imagerie par résonance magnétique , Syndromes oro-facio-digitauxRÉSUMÉ
BACKGROUND: Joubert syndrome (JS) belongs to the ciliopathies and is a mostly autosomal recessively inherited disease (in the case of OFD1 mutations, JS is an X-linked trait). It is characterised by midbrain-hindbrain malformations with developmental delay, hypotonia and ataxia and a broad spectrum of other facultative findings. The aim of our study was to examine the ophthalmological and neuro-ophthalmological features of JS in our patients and to compare our findings to those of other studies. METHODS: In a retrospective study we evaluated the ophthalmological and neuro-ophthalmological findings of 9 consecutive patients who met the diagnostic criteria of JS. RESULTS: All patients had abnormalities of ocular motility, 4/9 used head thrusts to shift gaze (oculomotor apraxia OMA). In 6/8 patients, the optokinetic reflex (OKN) was absent. Furthermore, 8/9 children showed nystagmus, mostly see-saw nystagmus. Manifest strabismus was found in 8/9 while 3/9 had a retinopathy with either abnormal ERG and/or fundus appearance with or without visual impairment. Chorioretinal colobomata were present in 5/9 cases. Two patients showed a unilateral congenital ptosis, one a facial nerve paresis. CONCLUSIONS: The early neuro-ophthalmological findings in JS are not pathognonomic, but may lead to the diagnosis of JS. The syndrome should be suspected in patients with nystagmus, especially see-saw nystagmus, and abnormal OKN and/or OMA, and/or colobomata of the fundus, and further paediatric examinations should be initiated.
Sujet(s)
Maladies du cervelet , Colobome , Polykystoses rénales , Protéines adaptatrices de la transduction du signal/génétique , Adolescent , Amblyopie/diagnostic , Amblyopie/génétique , Antigènes néoplasiques/génétique , Blépharoptose/diagnostic , Blépharoptose/génétique , Tronc cérébral/malformations , Tronc cérébral/anatomopathologie , Protéines du cycle cellulaire , Maladies du cervelet/classification , Maladies du cervelet/diagnostic , Maladies du cervelet/génétique , Cervelet/malformations , Cervelet/anatomopathologie , Enfant , Enfant d'âge préscolaire , Colobome/classification , Colobome/diagnostic , Colobome/génétique , Consanguinité , Protéines du cytosquelette , Analyse de mutations d'ADN , Électrorétinographie , Paralysie faciale/diagnostic , Paralysie faciale/génétique , Femelle , Fond de l'oeil , Humains , Imagerie par résonance magnétique , Mâle , Protéines membranaires/génétique , Protéines tumorales/génétique , Nystagmus optocinétique/génétique , Troubles de la motilité oculaire/diagnostic , Troubles de la motilité oculaire/génétique , Polykystoses rénales/classification , Polykystoses rénales/diagnostic , Polykystoses rénales/génétique , Réfraction oculaire , Études rétrospectives , Strabisme/diagnostic , Strabisme/génétique , Acuité visuelle , Jeune adulteRÉSUMÉ
OBJECTIVE: With conventional MRI and single-photon emission computed tomography (SPECT), accurate diagnosis and precise classification of cerebellar atrophy are often difficult. The objective was to verify the utility of MRI voxel-based morphometry (VBM) in combination with SPECT using easy Z-score imaging (eZIS) for diagnosing and classifying cerebellar atrophy. PATIENTS AND METHODS: We assessed gray matter atrophy using VBM and blood perfusion using SPECT with eZIS in fifteen patients with different types of cerebellar atrophy, such as the cerebellar variant of multiple system atrophy (MSA-C), spinocerebellar ataxia type 3 (SCA3), SCA6, and autoimmune cerebellar ataxia (AICA). RESULTS: In all five MSA-C patients, VBM imaging showed atrophy of the brainstem, the entire cerebellar vermis, and the cerebellar hemispheres, while SPECT using eZIS showed reduced perfusion in the same regions. Regarding SCA3, brainstem atrophy and reduced perfusion were recognized in two of the four patients, but none exhibited abnormal findings in the posterior lobe of the cerebellar vermis. SPECT showed that all four patients had obviously reduced perfusion in the anterior lobe of the vermis, but VBM demonstrated that there was no obvious atrophy of gray matter in any patient, meaning that the results of SPECT and VBM contradicted each other completely. All SCA6 and AICA patients exhibited atrophy and reduced perfusion in the cerebellar hemispheres but not in the brainstem. Only one AICA patient exhibited atrophy and reduced perfusion of the entire cerebellar vermis. CONCLUSION: VBM clearly showed characteristic gray matter atrophy in the cerebellum and brainstem in different pathological conditions, thus indicating its high degree of utility in diagnosing and classifying cerebellar atrophy in combination with SPECT using eZIS.
Sujet(s)
Maladies du cervelet/classification , Maladies du cervelet/imagerie diagnostique , Cervelet/imagerie diagnostique , Cervelet/anatomopathologie , Imagerie diagnostique/méthodes , Tomographie par émission monophotonique/méthodes , Atrophie/imagerie diagnostique , Atrophie/anatomopathologie , Tronc cérébral/imagerie diagnostique , Tronc cérébral/anatomopathologie , Ataxie cérébelleuse/imagerie diagnostique , Ataxie cérébelleuse/anatomopathologie , Humains , Imagerie par résonance magnétique , Ataxies spinocérébelleuses/imagerie diagnostique , Ataxies spinocérébelleuses/anatomopathologieRÉSUMÉ
Cerebellar malformations are increasingly diagnosed in the fetal period. Consequently, their consideration requires stressful and often critical decisions from both clinicians and families. This has resulted in an emergent need to understand better the impact of these early life lesions on child development. We performed a comprehensive literature search of studies describing neurodevelopmental outcomes of cerebellar malformations between January 1997 and December 2007. Overall, the data suggested that children with isolated inferior vermis hypoplasia (IVH) and mega cisterna magna (MCM) have a good developmental outcome, whereas children with molar tooth sign/Joubert syndrome, vermis hypoplasia, pontocerebellar hypoplasia (PCH) type II, and cerebellar agenesis experience moderate to severe global developmental delays. Reports for Dandy-Walker malformation (DWM) were conflicting; however, the presence of a normally lobulated vermis and the absence of associated brain anomalies were associated with a more favourable outcome. Finally, children with isolated cerebellar hypoplasia experienced fewer impairments. Important methodological limitations highlighted include a lack of standardized outcome measure use in 79% of studies and the predominant use of retrospective study designs (85%), with 40% limited to case reports or case-series. In summary, rigorous outcome studies describing the spectrum of disabilities in survivors are urgently needed to accurately delineate the long-term neurodevelopmental consequences of cerebellar malformations.
Sujet(s)
Maladies du cervelet/complications , Maladies du cervelet/anatomopathologie , Cervelet/malformations , Incapacités de développement/complications , Incapacités de développement/anatomopathologie , Maladies du cervelet/classification , Cervelet/anatomopathologie , Enfant , Enfant d'âge préscolaire , Femelle , Humains , Nourrisson , Nouveau-né , Mâle , Grossesse , Études rétrospectivesRÉSUMÉ
Joubert syndrome and related cerebellar disorders (JSRD) are a group of recessive congenital ataxia conditions usually showing neonatal hypotonia, dysregulated breathing rhythms, oculomotor apraxia, and mental retardation. The pathognomonic finding in JSRD is the unique molar tooth sign (MTS) on brain imaging. There is a tremendously broad spectrum of signs and symptoms mainly including kidney, retina, and liver disease, along with polydactyly and facial dysmorphisms. Here we propose a new diagnostic classification within JSRD that includes four major subtypes. To test this classification, we performed a systematic recruitment and genetic evaluation from a single referral center in Egypt. Thirteen families were identified, four showed evidence of linkage to one of the four known genetic loci, three showed novel AHI1 mutations, and nine were excluded from known loci. Each family could be classified into one of the four subtypes. This classification may thus be useful in the evaluation of patients with JSRD.
Sujet(s)
Maladies du cervelet/diagnostic , Maladies du cervelet/génétique , Cervelet/anatomopathologie , Cervelet/physiopathologie , Prédisposition génétique à une maladie/génétique , Mutation/génétique , Malformations multiples/génétique , Atrophie/génétique , Atrophie/anatomopathologie , Atrophie/physiopathologie , Maladies du cervelet/classification , Maladies chromosomiques/classification , Maladies chromosomiques/diagnostic , Maladies chromosomiques/génétique , Cartographie chromosomique , Analyse de mutations d'ADN , Égypte , Femelle , Dépistage génétique , Génotype , Humains , Maladies du rein/imagerie diagnostique , Maladies du rein/génétique , Maladies du rein/physiopathologie , Maladies du foie/imagerie diagnostique , Maladies du foie/génétique , Maladies du foie/physiopathologie , Imagerie par résonance magnétique , Mâle , Voies nerveuses/anatomopathologie , Voies nerveuses/physiopathologie , Phénotype , Valeur prédictive des tests , Dégénérescence de la rétine/génétique , Dégénérescence de la rétine/anatomopathologie , Dégénérescence de la rétine/physiopathologie , Syndrome , ÉchographieRÉSUMÉ
OBJECTIVE: To analyze preserved and impaired aspects of feedforward grip force control during cyclic arm movements with a hand-held object after cerebellar damage. METHODS: We tested eight subjects with unilateral or bilateral cerebellar pathologies and eight healthy control subjects. Participants performed cyclic vertical arm movements with a hand held instrumented object at three different speeds. RESULTS: Compared to controls, patients excerted increased grip forces. The minimum force ratio between grip force and load force was constant across all movement frequencies, suggesting that patients anticipated speed-related changes in load magnitudes by adjusting the grip force. Thus the scaling of grip force level to self-generated load magnitudes was preserved. The coupling between grip and load profiles was assessed by cross correlation analysis. Patients exhibited significantly decreased maximum coefficients of cross correlation implicating impaired anticipation of inertial load fluctuations. However feedforward control could be preserved, as obvious from zero time lags of the maximum cross correlation coefficient. CONCLUSIONS: Our findings suggest that cerebellar lesions affect the processing of predictive grip force modulation in anticipation of inertial loads. Our results add further evidence to the theoretical concept that the cerebellum implements internal feedforward models. However, preserved functions may indicate compensatory mechanisms or extra-cerebellar aspects of grip and load force regulation. SIGNIFICANCE: The observed dissociation of performance deficits may have direct clinical implication and may guide the development of individual therapeutic strategies for patients with cerebellar disorders.
Sujet(s)
Maladies du cervelet/physiopathologie , Force de la main/physiologie , Kinesthésie/physiologie , Troubles des habiletés motrices/physiopathologie , Performance psychomotrice/physiologie , Adulte , Sujet âgé , Phénomènes biomécaniques , Maladies du cervelet/classification , Maladies du cervelet/complications , Femelle , Gravitation , Humains , Mâle , Adulte d'âge moyen , Mouvement/physiologie , Valeur prédictive des tests , Statistiques comme sujet , Statistique non paramétrique , Mise en charge/physiologieRÉSUMÉ
Many diseases involve the cerebellum and produce ataxia, which is characterized by incoordination of balance, gait, extremity and eye movements, and dysarthria. Cerebellar lesions do not always manifest with ataxic motor syndromes, however. The cerebellar cognitive affective syndrome (CCAS) includes impairments in executive, visual-spatial, and linguistic abilities, with affective disturbance ranging from emotional blunting and depression, to disinhibition and psychotic features. The cognitive and psychiatric components of the CCAS, together with the ataxic motor disability of cerebellar disorders, are conceptualized within the dysmetria of thought hypothesis. This concept holds that a universal cerebellar transform facilitates automatic modulation of behavior around a homeostatic baseline, and the behavior being modulated is determined by the specificity of anatomic subcircuits, or loops, within the cerebrocerebellar system. Damage to the cerebellar component of the distributed neural circuit subserving sensorimotor, cognitive, and emotional processing disrupts the universal cerebellar transform, leading to the universal cerebellar impairment affecting the lesioned domain. The universal cerebellar impairment manifests as ataxia when the sensorimotor cerebellum is involved and as the CCAS when pathology is in the lateral hemisphere of the posterior cerebellum (involved in cognitive processing) or in the vermis (limbic cerebellum). Cognitive and emotional disorders may accompany cerebellar diseases or be their principal clinical presentation, and this has significance for the diagnosis and management of patients with cerebellar dysfunction.