This was followed by neurological symptoms and signs indicating a left sided upper cervical cord lesion. MRI showed an infarct at this site in the territory of the left posterior spinal artery. This ...

Interdiscip Neurosurg Adv Tech Case Manag. 2017; 7:47–49. AntwiP, GrantR, KuzmikG, AbbedK. “White cord syndrome” of acute hemiparesis after posterior cervical decompression and fusion for chronic ...

Posterior reversible encephalopathy syndrome is a neurological disorder characterized by swelling or inflammation in the brain. It’s often treatable if diagnosed quickly. Posterior reversible ...

Three varieties of alien hand syndrome have been reported, involving lesions of the corpus callosum alone, the corpus callosum plus dominant medial frontal cortex, and posterior cortical/subcortical ...

We report a case presented with uraemic encephalopathy and posterior reversible encephalopathy syndrome (PRES)-related symptoms, which showed recovery after haemodialysis although PRES with seizures ...

Background Finger extension weakness could be a presentation of either posterior interosseous nerve (PIN) syndrome or multifocal motor neuropathy (MMN). However, there is a delay in the diagnosis of ...

The diagnosis was posterior reversible encephalopathy syndrome (PRES), made after clinical examination and MRI (Figure). MRI showed cortical and subcortical FLAIR hyperintense signals involving the ...

126.com Purpose To describe the clinical manifestations and treatment outcomes in a retrospective case series of morning glory syndrome (MGS) associated with persistent ... with PHPV would appear as ...

Spinal cord stimulation is usually considered for patients who have chronic pain that has not been relieved by other conservative or surgical treatment methods. In the United States, pain conditions ...

Marfan syndrome is a congenital condition, meaning a person has it from birth. Physical signs sometimes present in infancy but more often show up later in childhood or adolescence. Marfan syndrome ...

Prader-Willi syndrome is caused by a genetic disorder of chromosome 15. It is a rare disorder present at birth that results in a number of physical, mental, and behavioral problems. A key feature of ...