Search engine for discovering works of Art, research articles, and books related to Art and Culture
Javascript must be enabled to continue!
Palatal myoclonus induced by extirpation of a cerebellar astrocytoma
View through CrossRef
✓ A 45-year-old woman developed a rare case of palatal myoclonus with no other neurological signs after undergoing extirpation of a small cerebellar low-grade astrocytoma that was located in the right dentate nucleus. The palatal myoclonus has persisted for 4 years after the operation. Magnetic resonance T2-weighted imaging revealed a high-intensity lesion in the left inferior olive. Palatal myoclonus associated with the removal of cerebellar tumors is unusuall but may easily be overlooked.
Journal of Neurosurgery Publishing Group (JNSPG)
Title: Palatal myoclonus induced by extirpation of a cerebellar astrocytoma
Description:
✓ A 45-year-old woman developed a rare case of palatal myoclonus with no other neurological signs after undergoing extirpation of a small cerebellar low-grade astrocytoma that was located in the right dentate nucleus.
The palatal myoclonus has persisted for 4 years after the operation.
Magnetic resonance T2-weighted imaging revealed a high-intensity lesion in the left inferior olive.
Palatal myoclonus associated with the removal of cerebellar tumors is unusuall but may easily be overlooked.
Related Results
Essential palatal myoclonus with spontaneous resolution: a rare case report
Essential palatal myoclonus with spontaneous resolution: a rare case report
Introduction and Importance:
Palatal myoclonus is a rare movement disorder characterized by involuntary, jerky movements of the soft palate and palatal musculature. It ...
ASSESSMENT OF RELATIONSHIP BETWEEN CLINICAL MANIFESTATION OF CHIARI MALFORMATION TYPE I AND CEREBELLAR TONSILS HERNIATION MEASUREMENT WITHIN THE FORAMEN MAGNUM
ASSESSMENT OF RELATIONSHIP BETWEEN CLINICAL MANIFESTATION OF CHIARI MALFORMATION TYPE I AND CEREBELLAR TONSILS HERNIATION MEASUREMENT WITHIN THE FORAMEN MAGNUM
ABSTRACT
Chiari malformation type I(CMI) is a common condition. It is a subject of controversy from diagnosis to the management (16). Classically the diagnosis is m...
Expression of delta-catenin is associated with progression of human astrocytoma
Expression of delta-catenin is associated with progression of human astrocytoma
AbstractBackgroundδ-Catenin (CTNND2), which encodes a scaffold protein in humans, has been found in a few malignancies. However, the expression pattern and contribution of δ-cateni...
Fetal cerebellar development: 3D morphometric analysis of fetal postmortem MRI among Chinese fetuses
Fetal cerebellar development: 3D morphometric analysis of fetal postmortem MRI among Chinese fetuses
AbstractThe development of the cerebellum starts from early gestational period and extends postnatal. Because of its protracted development, the cerebellum is susceptible to develo...
SGCE Myoclonus Dystonia: A Case Report
SGCE Myoclonus Dystonia: A Case Report
BACKGROUND: SGCE myoclonus dystonia is a rare genetic movement disorder caused by mutations in the SGCE gene. It typically presents in childhood and is characterized by myoclonus a...