Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Parkinson Disease l: Introduction01:24

Parkinson Disease l: Introduction

Parkinson’s disease is a chronic, progressive neurodegenerative disorder that primarily affects movement. It is characterized by motor symptoms such as resting tremors, muscle rigidity, bradykinesia (slowness of movement), and postural instability. Patients may notice hand tremors at rest, stiffness during movement, or a shuffling gait. In addition to motor features, non-motor symptoms include sleep disturbances, mood and behavioral changes, constipation, and cognitive impairment, all of which...
Parkinson Disease ll: Pathophysiology01:24

Parkinson Disease ll: Pathophysiology

Parkinson disease (PD) is a progressive neurodegenerative disorder primarily affecting movement, with additional non-motor features. Its pathophysiology involves complex interactions among genetic susceptibility, environmental exposures, and cellular dysfunction, including dopaminergic neuron loss, protein aggregation, and mitochondrial impairment.Selective NeurodegenerationA key feature is the degeneration of dopaminergic neurons in the substantia nigra pars compacta, leading to reduced...
Parkinson's Disease: Overview01:15

Parkinson's Disease: Overview

Neurodegenerative disorders are progressive diseases that cause irreversible damage and loss to neurons in specific brain areas. Examples of these disorders include Parkinson's disease, Alzheimer's disease, Multiple Sclerosis (MS), and Amyotrophic Lateral Sclerosis (ALS). These disorders share characteristics such as proteinopathies, selective neuronal vulnerability, and a complex interplay between genetic and environmental factors. The primary therapeutic goal for these conditions is to...
Human Genetics01:28

Human Genetics

Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
Parkinson's Disease: Treatment01:24

Parkinson's Disease: Treatment

Neurodegenerative disorders, such as Parkinson's Disease (PD), involve the gradual and irreversible destruction of neurons in particular brain areas. These disorders exhibit standard features like proteinopathies, selective vulnerability of some neurons, and an interaction of intrinsic properties, genetics, and environmental influences in neural injury.
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of its...
Incomplete Dominance01:43

Incomplete Dominance

Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Atypical Perfusion Manifestation in Migraine with Aura.

Case reports in neurology·2021
Same author

Impaired glucose tolerance with neurological manifestations in insulinoma.

Clinical case reports·2021
Same author

Stiff Person Syndrome and Acetylcholine Receptor Ganglionic Neuronal Antibodies.

Case reports in neurology·2020
Same author

Treatment with Botulinum Toxin for Refractory Fever Caused by Severe Spasticity: A Case Series.

Neurology and therapy·2018
Same author

Hiccup secondary to dopamine agonists in Parkinson's disease.

Movement disorders : official journal of the Movement Disorder Society·2007
Same author

Diffuse intracranial calcinosis: Fahr disease.

Archives of neurology·2006

Related Experiment Video

Updated: Jul 19, 2026

The Use of Primary Human Fibroblasts for Monitoring Mitochondrial Phenotypes in the Field of Parkinson's Disease
15:09

The Use of Primary Human Fibroblasts for Monitoring Mitochondrial Phenotypes in the Field of Parkinson's Disease

Published on: October 3, 2012

Parkinson's disease and genetics.

Jacobo Lester1, Enrique Otero-Siliceo

  • 1Hospital de Clínicas José de San Martín, Huixquilucan, Estado de México, Mexico. jacobolester@hotmail.com

The Neurologist
|September 23, 2006
PubMed
Summary

Genetic factors are increasingly implicated in the etiology of idiopathic Parkinson disease (IPD). This review examines epidemiological and twin studies to explore the genetic links to Parkinson disease.

Area of Science:

  • Neurology
  • Genetics
  • Epidemiology

Background:

  • Idiopathic Parkinson disease (IPD) is a neurodegenerative disorder with an unknown cause.
  • Multiple factors are suspected to contribute to IPD onset.
  • Research is ongoing to identify the specific etiology of Parkinson disease.

Purpose of the Study:

  • To review significant studies investigating the relationship between genetics and Parkinson disease.
  • To present current epidemiological findings related to Parkinson disease.
  • To highlight key genetic factors implicated in Parkinson disease.

Main Methods:

  • Review of epidemiological studies on Parkinson disease.
  • Analysis of twin studies examining genetic mutations in Parkinson disease families.

More Related Videos

Gene-environment Interaction Models to Unmask Susceptibility Mechanisms in Parkinson's Disease
08:09

Gene-environment Interaction Models to Unmask Susceptibility Mechanisms in Parkinson's Disease

Published on: January 7, 2014

Related Experiment Videos

Last Updated: Jul 19, 2026

The Use of Primary Human Fibroblasts for Monitoring Mitochondrial Phenotypes in the Field of Parkinson's Disease
15:09

The Use of Primary Human Fibroblasts for Monitoring Mitochondrial Phenotypes in the Field of Parkinson's Disease

Published on: October 3, 2012

Gene-environment Interaction Models to Unmask Susceptibility Mechanisms in Parkinson's Disease
08:09

Gene-environment Interaction Models to Unmask Susceptibility Mechanisms in Parkinson's Disease

Published on: January 7, 2014

  • Synthesis of current research on genetic factors and Parkinson disease.
  • Main Results:

    • Genetic factors are recognized as significant in explaining Parkinson disease onset.
    • Studies are categorized into epidemiological and family-based genetic analyses.
    • Evidence linking specific genetic mutations to Parkinson disease is accumulating.

    Conclusions:

    • Epidemiological studies provide insights into Parkinson disease prevalence and risk factors.
    • Key genetic factors contributing to Parkinson disease are identified.
    • The review incorporates the latest available information on genetics and Parkinson disease.