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Disorders of the Nervous Tissue01:28

Disorders of the Nervous Tissue

Nervous tissue is a vital component of the human body's communication system, enabling us to perceive and respond to stimuli. However, like all other tissues, it is vulnerable to disorders and diseases that can significantly impact our neurological functioning.
Homeostatic Imbalances:
Alzheimer's disease manifests as a gradual decline in memory and cognitive abilities, attributed to the buildup of amyloid plaques and neurofibrillary tangles in the brain.
Parkinson's disease arises from the...
Diphtheria01:28

Diphtheria

Diphtheria is an acute, toxin-mediated infectious disease that primarily affects the upper respiratory tract. It is caused by Corynebacterium diphtheriae, a Gram-positive, pleomorphic rod that lacks spore-forming capability and exhibits a characteristic club-shaped morphology under microscopic examination. While C. diphtheriae can asymptomatically colonize mucosal surfaces, clinical disease manifests only when the bacterial strain is lysogenized by a specific β-corynephage. This phage...
Multiple Sclerosis l: Introduction01:19

Multiple Sclerosis l: Introduction

Multiple sclerosis is a chronic autoimmune disease of the central nervous system (CNS) that affects the brain, spinal cord, and optic nerves. It is an inflammatory demyelinating disorder and a leading cause of neurological disability in young adults.EpidemiologyMS commonly begins between 20 and 40 years of age and is twice as common in women. Its exact cause remains unclear, but genetic susceptibility contributes, with higher risk in first-degree relatives and identical twins. A greater...
Arboviral Encephalitis01:25

Arboviral Encephalitis

Arboviral encephalitis refers to brain inflammation caused by arthropod-borne viruses, particularly those transmitted through mosquito vectors. Among these, West Nile virus (WNV), a member of the Flaviviridae family, is a significant public health concern. WNV is an enveloped, positive-sense, single-stranded RNA virus. Human infection typically begins when an infected mosquito introduces the virus into the dermis during feeding. The primary transmission cycle involves birds as amplifying hosts...
Hepatic Encephalopathy01:29

Hepatic Encephalopathy

DefinitionHepatic encephalopathy is a reversible neurologic syndrome that results from advanced liver dysfunction or portosystemic shunting. It leads to disturbances in cognition, behavior, and motor function due to the brain’s exposure to gut-derived toxins that the liver fails to detoxify.EtiologyThis condition develops either in the setting of acute fulminant hepatitis or progressively during chronic liver disease, such as cirrhosis and portal hypertension. Portosystemic shunting—including...
Huntington Disease l: Introduction01:21

Huntington Disease l: Introduction

Huntington disease or HD is a progressive, fatal neurodegenerative disorder inherited in an autosomal dominant pattern.PathophysiologyIt is caused by expansion of the CAG trinucleotide repeat in the HTT gene on chromosome 4 (4p16.3), producing an abnormal huntingtin protein with an expanded polyglutamine tract. This misfolded protein disrupts cellular function, leading to neuronal death. Normal alleles have ≤26 repeats, 27–35 are intermediate (risk of expansion), 36–39 show reduced penetrance,...

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Related Experiment Video

Updated: Jun 16, 2026

Nerve Ultrasound Protocol to Detect Dysimmune Neuropathies
08:56

Nerve Ultrasound Protocol to Detect Dysimmune Neuropathies

Published on: October 7, 2021

Neurologic Wilson's disease.

Matthew T Lorincz1

  • 1Department of Neurology, University of Michigan Health Systems, Ann Arbor, Michigan, USA. Lorincz@umich.edu

Annals of the New York Academy of Sciences
|February 12, 2010
PubMed
Summary

Wilson's disease, a genetic disorder of copper metabolism, is often misdiagnosed. Early diagnosis and treatment of this neurodegenerative condition can prevent severe disability and ensure a normal lifespan.

Area of Science:

  • Genetics and Neurology
  • Metabolic Disorders

Background:

  • Wilson's disease is an inherited autosomal recessive disorder resulting from mutations in the ATP7B gene.
  • It leads to impaired copper metabolism, causing toxic copper accumulation in various organs, particularly the brain and liver.
  • Neurologic Wilson's disease presents with a range of symptoms including dysarthria, dystonia, tremor, and choreoathetosis.

Purpose of the Study:

  • To review the key neurologic manifestations of Wilson's disease.
  • To discuss diagnostic strategies for Wilson's disease.
  • To outline current and emerging treatment options for Wilson's disease.

Main Methods:

  • Literature review focusing on neurologic Wilson's disease.
  • Analysis of diagnostic criteria and methods.

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Lipidomics and Transcriptomics in Neurological Diseases
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Lipidomics and Transcriptomics in Neurological Diseases

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Lipidomics and Transcriptomics in Neurological Diseases
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Lipidomics and Transcriptomics in Neurological Diseases

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  • Examination of therapeutic interventions and their outcomes.
  • Main Results:

    • Wilson's disease is frequently misdiagnosed, delaying critical treatment.
    • Neurologic symptoms are highly variable, complicating early identification.
    • Timely and appropriate treatment can halt disease progression and reverse symptoms, leading to normal life expectancy.

    Conclusions:

    • Wilson's disease is a treatable neurodegenerative disorder with significant implications of delayed diagnosis.
    • Increased awareness and improved diagnostic approaches are crucial for affected individuals.
    • Effective management can prevent irreversible hepatic failure and severe neurologic disability.