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 Experiment Videos

Encephalocraniocutaneous lipomatosis.

M A Fishman

    Journal of Child Neurology
    |July 1, 1987
    PubMed
    Summary
    This summary is machine-generated.

    Encephalocraniocutaneous lipomatosis involves brain abnormalities and head skin lesions. Progressive neurological issues suggest a primary defect in embryonic tissue development.

    Related Concept Videos

    You might also read

    Related Articles

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

    Sort by
    Same author

    Selective loss of myelin proteins during autolysis.

    Neurochemical research·2013
    Same author

    Selective decrease of S-100 in discrete anatomical areas of undernourished rat brain.

    Neurochemical research·2013
    Same author

    Th1/Th2 differentiation and cross-regulation.

    Bulletin of mathematical biology·2007
    Same author

    Heterogeneity stabilizes reciprocal altruism interactions.

    Journal of theoretical biology·2001
    Same author

    Neck-tongue syndrome.

    Pediatric neurology·2000
    Same author

    Evolution of cooperation between individuals.

    Nature·1999
    Same journal

    Neuromuscular Symptoms of <i>ORAI1</i>-Related Immunodeficiency.

    Journal of child neurology·2026
    Same journal

    Symptoms of Obsessive-Compulsive Disorder, Attention-Deficit/Hyperactivity Disorder, and Autism Spectrum Disorder in Children and Adolescents Attending a Headache Outpatient Clinic and School-Based Controls.

    Journal of child neurology·2026
    Same journal

    Acute Encephalopathy From Central Nervous System Hemophagocytic Lymphohistiocytosis (CNS HLH) in X-Linked Lymphoproliferative Disease Type 1 (XLP-1).

    Journal of child neurology·2026
    Same journal

    The Cost of Fear for Pediatric Neurologic Care.

    Journal of child neurology·2026
    Same journal

    Hospitalisation Experiences of Children with Neurological Illness: A Qualitative Exploration.

    Journal of child neurology·2026
    Same journal

    The Burden of Idiopathic Developmental Intellectual Disability Attributed to Lead Exposure in Asian Children and Adolescents, 1990-2021: Trends, Inequalities, and Future Projections for the Global Burden of Disease Study 2021.

    Journal of child neurology·2026
    See all related articles

    Area of Science:

    • Neurology
    • Medical Genetics
    • Developmental Biology

    Background:

    • Encephalocraniocutaneous lipomatosis (ECCL) is a rare congenital disorder.
    • Characterized by unilateral brain malformations and ipsilateral craniofacial abnormalities.

    Observation:

    • Cutaneous manifestations include lipomas affecting the scalp, face, and eyes.
    • Neurological findings encompass cerebral hemiatrophy, porencephaly, and defective insular opercularization.
    • Lesions and clinical symptoms show progressive deterioration.

    Findings:

    • The progressive nature and apparent vascular pathogenesis of intracranial lesions are noted.
    • Suggests a primary defect in embryonic mesenchyme-derived tissues.
    • Secondary involvement of ectoderm-derived tissues is proposed.

    Related Experiment Videos

    Implications:

    • Understanding the pathogenesis of ECCL is crucial for diagnosis and management.
    • Further research into the vascular and developmental mechanisms is warranted.
    • Highlights the complex interplay between mesenchyme and ectoderm in neurodevelopmental disorders.