Ataxic Gait
View article: A case report of CLIPPERS syndrome with gait and cognitive impairment
A case report of CLIPPERS syndrome with gait and cognitive impairment Open
CLIPPERS syndrome should be considered in patients presenting with subacute pontocerebellar dysfunction and characteristic MRI findings. Early diagnosis and prompt corticosteroid therapy can lead to favorable outcomes. Long-term immunosupp…
View article: Longitudinal Effects of Bilateral Subthalamic Nucleus Deep Brain Stimulation Versus Best Medical Therapy on Static and Dynamic Balance and Gait in Advanced Parkinson’s Disease: A 36-Month Comparative Study
Longitudinal Effects of Bilateral Subthalamic Nucleus Deep Brain Stimulation Versus Best Medical Therapy on Static and Dynamic Balance and Gait in Advanced Parkinson’s Disease: A 36-Month Comparative Study Open
Objective: To evaluate the long-term impact of bilateral subthalamic nucleus deep brain stimulation (STN-DBS) versus best medical therapy (BMT) on static and dynamic balance as well as gait disturbances in patients with advanced Parkinson’…
View article: Concurrent <scp>ANNPE</scp> and vertebral T‐cell lymphoma in a dog: A case report
Concurrent <span>ANNPE</span> and vertebral T‐cell lymphoma in a dog: A case report Open
Acute non‐compressive nucleus pulposus extrusion (ANNPE) is a recognised cause of peracute spinal cord injury in dogs, involving sudden extrusion of non‐degenerated nucleus pulposus with minimal compression. While often linked to vigorous …
View article: Hyperkinetic Movement Disorder Emergencies: A Retrospective Study From China
Hyperkinetic Movement Disorder Emergencies: A Retrospective Study From China Open
Introduction Movement disorders, especially hyperkinetic movement disorders, can present in emergency services in an acute and/or severe form and are aetiologically heterogeneous. Because limited data exist on the epidemiology and clinical…
View article: Early-Onset Ataxia with Oculo-Motor Apraxia and Hypoalbuminemia – A Rare Case Report from South Indian Region
Early-Onset Ataxia with Oculo-Motor Apraxia and Hypoalbuminemia – A Rare Case Report from South Indian Region Open
Neurodegenerative diseases commonly manifest as progressive deterioration of neurological function in varied forms. Damage to the cerebellum disrupts the coordination of limb and eye movements, impairs balance, and decreases muscle tone. A…
View article: CERG-06 FROM IMPOSSIBLE TO FEASIBLE : SUCCESSFUL LAUNCH OF SURGERY FOR INTRACRANIAL TUMORS AT THE BOUAKE CHR
CERG-06 FROM IMPOSSIBLE TO FEASIBLE : SUCCESSFUL LAUNCH OF SURGERY FOR INTRACRANIAL TUMORS AT THE BOUAKE CHR Open
Introduction Neurosurgery is an emerging discipline in several African hospitals. In Ivory Coast, the city of Bouaké could represent a pioneering center in the management of neurosurgical pathologies, particularly tumors, since the advent …
View article: Наследственные атаксии, протекающие под маской детского церебрального паралича
Наследственные атаксии, протекающие под маской детского церебрального паралича Open
Introduction. Ataxic cerebral palsy (CP) is the least common of all forms of CP, occurring in less than 1 in 10 CP patients. By the age of 5 years, more than half of these children have their diagnosis reconsidered and other conditions not…
View article: Gut-Feeling: A Cerebellar Infarct Masquerading as Gastrointestinal Illness
Gut-Feeling: A Cerebellar Infarct Masquerading as Gastrointestinal Illness Open
Title Gut-Feeling: A Cerebellar Infarct Masquerading as Gastrointestinal Illness Background Posterior circulation strokes, particularly those involving the cerebellum, can present with non-specific symptoms such as vertigo, nausea, vomitin…
View article: Case Report: Unmasked: Deceptive pediatric spinal meningioma
Case Report: Unmasked: Deceptive pediatric spinal meningioma Open
Introduction Pediatric meningiomas are rare tumors originating from the meninges’ arachnoid cap cells, representing a small fraction of all meningiomas. The clinical presentation of pediatric meningiomas varies widely depending on their lo…
View article: Severe Elimination Disorders and Normal Intelligence in a Case of MAP1B Related Syndrome: A Case Report
Severe Elimination Disorders and Normal Intelligence in a Case of MAP1B Related Syndrome: A Case Report Open
Pathogenic variants in the MAP1B gene have been associated with neurological impairment, including intellectual disability, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, brain malformations, cognitive hearing l…
View article: An Imitation-Based Treatment for Ataxic Dysarthria: A Retrospective Multiple Single-Case Study
An Imitation-Based Treatment for Ataxic Dysarthria: A Retrospective Multiple Single-Case Study Open
Background/Objectives: Ataxic dysarthria is a speech disorder characterized by the impaired coordination of movement due to cerebellar dysfunction. Despite its clinical relevance, few studies have explored its rehabilitation. This study ai…
View article: POLR3A rare variants in a patient with intellectual disability, ataxic gait and cortical malformations: a case-report
POLR3A rare variants in a patient with intellectual disability, ataxic gait and cortical malformations: a case-report Open
View article: Change in the Location of a Pseudotumor Around the C2 Odontoid Process from Posterior to Anterior to the Odontoid Process in the Natural Course: A Case with “Antero-Odontoid Pseudotumor” or “Peri-Odontoid Pseudotumor”
Change in the Location of a Pseudotumor Around the C2 Odontoid Process from Posterior to Anterior to the Odontoid Process in the Natural Course: A Case with “Antero-Odontoid Pseudotumor” or “Peri-Odontoid Pseudotumor” Open
Background: A pseudotumor adjacent to the odontoid has been reported to be a non-neoplastic mass that is mainly associated with atlantoaxial instability. Methods: Case report. Results: A 72-year-old woman presented to our clinic with a chi…
View article: Radiological features of gait phenotypes in patients with idiopathic normal pressure hydrocephalus
Radiological features of gait phenotypes in patients with idiopathic normal pressure hydrocephalus Open
Introduction According to the higher-level gait disorder (HLGD) pattern, patients with idiopathic normal pressure hydrocephalus (iNPH) can be divided into two motor phenotypes; a disequilibrium (wide-based gait) subtype and a parkinsonian …
View article: Bilateral vestibulopathy in Alexander disease type II– a case report
Bilateral vestibulopathy in Alexander disease type II– a case report Open
View article: Characteristics of children with ataxic cerebral palsy
Characteristics of children with ataxic cerebral palsy Open
View article: Massive cerebellar infarction caused by spontaneously isolated posterior inferior cerebellar artery dissection: A case report
Massive cerebellar infarction caused by spontaneously isolated posterior inferior cerebellar artery dissection: A case report Open
BACKGROUND Diagnosing posterior inferior cerebellar artery dissection (PICAD) using radiological images is challenging. Massive cerebellar infarctions resulting from spontaneous, isolated PICAD are rare, and the associated clinical, imagin…
View article: Case Report of Myoclonus‐Ataxia Syndrome in an Indian Patient Due to <scp><i>SCNA1</i></scp> Gene Mutation
Case Report of Myoclonus‐Ataxia Syndrome in an Indian Patient Due to <span><i>SCNA1</i></span> Gene Mutation Open
View article: Influence of Robotic Neurorehabilitation in Cerebral Palsy on Motor Function and Gait
Influence of Robotic Neurorehabilitation in Cerebral Palsy on Motor Function and Gait Open
Background and aim: Cerebral palsy (CP) is a nonprogressive neurological disorder characterized by permanent developmental disorders of movement and posture. One of the most common goals of rehabilitation is the treatment of gait disorders…
View article: Ataxia telangiectasia in a Bahraini child treated with intensive physiotherapy: A case report
Ataxia telangiectasia in a Bahraini child treated with intensive physiotherapy: A case report Open
Ataxia telangiectasia (AT) is a rare neurodegenerative condition with a prevalence of 1 in 40,000 to 1 in 300,000 worldwide. It involves a genetic mutation of chromosome 11q.26. The condition is inherited in an autosomal recessive manner c…
View article: A novel early onset spinocerebellar ataxia 13 BAC mouse model with cerebellar atrophy, tremor, and ataxic gait
A novel early onset spinocerebellar ataxia 13 BAC mouse model with cerebellar atrophy, tremor, and ataxic gait Open
Spinocerebellar ataxia 13 (SCA13) is an autosomal dominant neurological disorder caused by mutations in KCNC3. Our previous studies revealed that KCNC3 (Potassium Voltage-Gated Channel Subfamily C Member 3) mutation R423H results in an ear…
View article: Oculodentodigital Dysplasia Presenting as Spastic Ataxic Syndrome in an Indian Patient
Oculodentodigital Dysplasia Presenting as Spastic Ataxic Syndrome in an Indian Patient Open
Spastic ataxic syndrome is a combination of cerebellar ataxia with spasticity and other pyramidal features. Common causes of spastic ataxic syndrome include spinocerebellar ataxia (SCA) 1, SCA2, autosomal recessive ataxia of Charlevoix–Sag…
View article: A rare case of recurrent spinal hydatid cyst in a 17-year-old man with neurological deficits and balance impairment
A rare case of recurrent spinal hydatid cyst in a 17-year-old man with neurological deficits and balance impairment Open
Patients with spinal hydatidosis often exhibit spinal cord compression symptoms. When imaging modalities reveal multiple cysts and there is a history of residency in an endemic area, spinal hydatid cyst should be considered. Although rare,…
View article: Unsupported walking with only half of the brain due to severe porencephaly
Unsupported walking with only half of the brain due to severe porencephaly Open
A BSTRACT A patient with a history of Asian flu, mumps meningo-encephalitis, and skull-base fracture and severe porencephaly who was able to walk without assistance, has not been reported. The patient is a 65 year-old male with a history o…
View article: A rare case of hypertrophic olivary degeneration in a patient with pontine hemorrhage
A rare case of hypertrophic olivary degeneration in a patient with pontine hemorrhage Open
Introduction and aim. Hypertrophic olivary degeneration (HOD) is an extremely rare disease that affects the inferior olivary nucleus (ION) in the medulla oblongata and is also referred to as hypertrophic degeneration of the inferior olives…
View article: Utilization of Motor Imagery Training for Improvement of Balance of Ataxic Children after Medulloblastoma Resection
Utilization of Motor Imagery Training for Improvement of Balance of Ataxic Children after Medulloblastoma Resection Open
This study investigated the effects of training using motor imagery on balance, gait parameters, and ataxia severity in children after they underwent medulloblastoma tumour resection. Fifty participated children, aged seven-nine years and …
View article: New onset of ataxic dysarthria with CSF overdrainage syndrome: A case report
New onset of ataxic dysarthria with CSF overdrainage syndrome: A case report Open
Cerebrospinal fluid (CSF) overdrainage syndrome occurs when excessive CSF drainage from the cranial cavity results from a spinal CSF leak or overdrainage through a ventriculoperitoneal (VP) or lumboperitoneal (LP) shunt. Symptoms include s…
View article: AtGCN: A Graph Convolutional Network For Ataxic Gait Detection
AtGCN: A Graph Convolutional Network For Ataxic Gait Detection Open
Video-based gait analysis can be defined as the task of diagnosing pathologies, such as ataxia, using videos of patients walking in front of a camera. This paper presents a graph convolution network called AtGCN for detecting ataxic gait a…
View article: A Novel Early Onset Spinocerebellar Ataxia 13 BAC Mouse Model with Cerebellar Hypoplasia, Tremor, and Ataxic Gait
A Novel Early Onset Spinocerebellar Ataxia 13 BAC Mouse Model with Cerebellar Hypoplasia, Tremor, and Ataxic Gait Open
Spinocerebellar ataxia 13 (SCA13) is an autosomal dominant neurological disorder caused by mutations in KCNC3 . Our previous studies revealed that KCNC3 mutation R423H results in an early-onset form of SCA13. Previous biological models of …
View article: Utilization of Robot-Assisted Gait Training in Pulmonary Rehabilitation for a Patient with Ambulatory Dysfunction Post-Severe COVID-19 Pneumonia: A Case Report
Utilization of Robot-Assisted Gait Training in Pulmonary Rehabilitation for a Patient with Ambulatory Dysfunction Post-Severe COVID-19 Pneumonia: A Case Report Open
Background: Severe COVID-19 can lead to a decline in pulmonary and physical functions simultaneously. Patients experiencing significant ambulatory dysfunction often face restrictions in participating in gait training, resulting in insuffic…