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

Epistasis Analysis01:09

Epistasis Analysis

Although Mendel chose seven unrelated traits in peas to study gene segregation, most traits involve multiple gene interactions that create a spectrum of phenotypes. When the interaction of various genes or alleles at different locations influences a phenotype, this is called epistasis. Epistasis often involves one gene masking or interfering with the expression of another (antagonistic epistasis). Epistasis often occurs when different genes are part of the same biochemical pathway. The...
Lethal Alleles02:41

Lethal Alleles

Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
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.
Anorexia Nervosa01:28

Anorexia Nervosa

Anorexia nervosa is a complex and severe eating disorder characterized by an intense fear of weight gain, an unrelenting pursuit of thinness, and a distorted body image. It often leads to dangerously low body weight relative to an individual's age and height. This disorder is marked by significant physical and psychological consequences, making it one of the most life-threatening psychiatric illnesses.
Symptoms and Physical Effects
Individuals with anorexia nervosa commonly exhibit extreme...
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...
Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...

You might also read

Related Articles

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

Sort by
Same author

Post-infection sequelae of COVID-19 and other infectious diseases-a nationwide Danish study with 40-month follow-up.

Nature communications·2026
Same author

Treatment-Limiting Decisions in Neurointensive Care: Withholding or Withdrawal of Life-Sustaining Measures.

Acta anaesthesiologica Scandinavica·2026
Same author

Reply to 'Recalled experiences of death: need for empirical research without prejudice'.

Nature reviews. Neurology·2026
Same author

Acute non-alcoholic nutritional neuropathies in high-income countries - a systematic review.

Danish medical journal·2025
Same author

Covert consciousness: what's in a name?

Brain : a journal of neurology·2025
Same author

Spontaneous Eye Blinking as a Potential Clinical Marker for Arousal in the Intensive Care Unit.

Neurocritical care·2025

Related Experiment Video

Updated: May 30, 2026

A Scalable, Cell-Based Method for the Functional Assessment of Ube3a Variants
06:35

A Scalable, Cell-Based Method for the Functional Assessment of Ube3a Variants

Published on: October 10, 2022

Anton's syndrome and eugenics.

Daniel Kondziella1, Siska Frahm-Falkenberg

  • 1Department of Neurology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Journal of Clinical Neurology (Seoul, Korea)
|July 23, 2011
PubMed
Summary
This summary is machine-generated.

Anton's syndrome, a striking form of anosognosia, involves patients denying blindness. This paper reviews Anton's syndrome and Gabriel Anton's broader, often overlooked, contributions and problematic eugenics advocacy.

Keywords:
Nazianosognosiacerebral infarctiondisconnection syndromeendocarditiseuthanasiaracial hygiene

More Related Videos

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
05:51

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane
07:38

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane

Published on: March 30, 2015

Related Experiment Videos

Last Updated: May 30, 2026

A Scalable, Cell-Based Method for the Functional Assessment of Ube3a Variants
06:35

A Scalable, Cell-Based Method for the Functional Assessment of Ube3a Variants

Published on: October 10, 2022

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
05:51

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane
07:38

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane

Published on: March 30, 2015

Area of Science:

  • Neuroscience
  • Clinical Neurology
  • History of Medicine

Background:

  • Anton's syndrome is a profound neurological condition characterized by anosognosia, specifically visual anosognosia where patients deny their blindness.
  • Gabriel Anton, a neurologist, is recognized for his work on anosognosia, asomatognosia, neurosurgery, neuropsychology, and child psychiatry.

Purpose of the Study:

  • To present a case study of Anton's syndrome.
  • To contextualize Gabriel Anton's contributions to clinical neurosciences.
  • To highlight Anton's unrecognized advocacy for eugenics and racial hygiene.

Main Methods:

  • Case study presentation.
  • Historical review of Gabriel Anton's published works and advocacy.
  • Analysis of Anton's syndrome within its historical and scientific context.

Main Results:

  • The paper details a case of Anton's syndrome, illustrating the phenomenon of visual anosognosia.
  • Gabriel Anton's significant, yet less recognized, contributions to neurosurgery, neuropsychology, and child psychiatry are discussed.
  • Anton's historical advocacy for eugenics and racial hygiene, previously under-reported in English literature, is examined.

Conclusions:

  • Anton's syndrome remains a compelling example of anosognosia, underscoring the complexities of self-awareness in neurological disorders.
  • A comprehensive understanding of Gabriel Anton requires acknowledging both his neuroscientific advancements and his problematic eugenic views.
  • This work provides historical context for Anton's syndrome and the broader legacy of Gabriel Anton.