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Related Concept Videos

Pleiotropy01:33

Pleiotropy

Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
Sex-linked Disorders01:43

Sex-linked Disorders

Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
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...
Sex Linked Disorders01:43

Sex Linked Disorders

Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
Lateralization01:28

Lateralization

Brain lateralization refers to the division of mental processes and functions between the two hemispheres of the brain, a phenomenon that optimizes neural efficiency and underpins complex abilities in humans. This specialization allows each hemisphere to perform tasks where it has a comparative advantage, facilitating more refined cognitive capabilities across different domains.
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 8, 2026

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis
08:16

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis

Published on: March 4, 2014

The pathological left-handedness syndrome.

P Satz, D L Orsini, E Saslow

    Brain and Cognition
    |January 1, 1985
    PubMed
    Summary

    Pathological left-handedness (PLH) is a proposed syndrome linked to early left-brain injury before age 6. This condition in left-handers involves developmental changes impacting handedness, speech, and spatial cognition.

    Area of Science:

    • Neuroscience
    • Developmental Psychology
    • Clinical Neurology

    Background:

    • Early brain injury can affect lateralization and cognitive development.
    • Left-handedness is sometimes associated with atypical brain organization.
    • Previous research has identified some correlates of brain injury in left-handers, but not as a distinct syndrome.

    Purpose of the Study:

    • To propose and define a clinical syndrome of pathological left-handedness (PLH).
    • To identify the pattern of lateral developmental changes associated with early brain injury in left-handers.
    • To explore the implications of recognizing PLH for diagnosis, remediation, and understanding functional recovery.

    Main Methods:

    • Clinical observation and analysis of developmental patterns in manifest left-handers.

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    Block Building Task Identifies Distinct Groups of Left/Right-hand Choice Patterns After Unilateral Peripheral Nerve Injury
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    Block Building Task Identifies Distinct Groups of Left/Right-hand Choice Patterns After Unilateral Peripheral Nerve Injury

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    Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis
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    Published on: March 4, 2014

    Evaluation of Hemisphere Lateralization with Bilateral Local Field Potential Recording in Secondary Motor Cortex of Mice
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    Block Building Task Identifies Distinct Groups of Left/Right-hand Choice Patterns After Unilateral Peripheral Nerve Injury
    07:06

    Block Building Task Identifies Distinct Groups of Left/Right-hand Choice Patterns After Unilateral Peripheral Nerve Injury

    Published on: March 21, 2025

  • Correlation of specific neurological and cognitive features with early hemispheric lesions.
  • Review of existing literature on lateral development and brain injury.
  • Main Results:

    • Pathological left-handedness (PLH) is characterized by a pattern of correlative changes in lateral development.
    • These changes result from early (before age 6) left-sided or asymmetric brain lesions affecting speech zones.
    • Manifestations include shifts in manual dominance, extremity changes, speech transfer, and visuospatial reorganization.

    Conclusions:

    • PLH represents a recognizable clinical syndrome in manifest left-handers with early brain injury.
    • Identifying PLH has significant implications for clinical diagnosis and intervention strategies.
    • Understanding PLH contributes to models of brain plasticity and recovery of function.