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

[Hereditary acrokeratotic poikiloderma].

S Pons, R N Billene, A Ortiz

    Medicina Cutanea Ibero-Latino-Americana
    |January 1, 1975
    PubMed
    Summary
    This summary is machine-generated.

    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

    HD-MUNet: integrating artificial intelligence and high-density electromyography for motor unit number estimation.

    IEEE transactions on bio-medical engineering·2026
    Same author

    Comparison of 2 swept-source optical biometers: IOLMaster 700 vs. Revo FC 130.

    Archivos de la Sociedad Espanola de Oftalmologia·2025
    Same author

    Good clinical practice recommendations for the management of gastroesophageal reflux disease. A Latin American expert review.

    Revista de gastroenterologia de Mexico (English)·2025
    Same author

    Post-traumatic retinal siderosis, a case report.

    Archivos de la Sociedad Espanola de Oftalmologia·2024
    Same author

    Effectiveness of handheld near infrared spectrometer for traceability of Angus steaks.

    Food chemistry·2024
    Same author

    Progressive supranuclear palsy, a case report.

    Archivos de la Sociedad Espanola de Oftalmologia·2024
    Same journal

    [Acquired bullous epidermolysis and multiple myeloma].

    Medicina cutanea ibero-latino-americana·1990
    Same journal

    [Eosinophilic ulcer of the tongue. Pathogenic role of eosinophils].

    Medicina cutanea ibero-latino-americana·1990
    Same journal

    [Facial granuloma caused by cactus bristles].

    Medicina cutanea ibero-latino-americana·1990
    Same journal

    [Epithelioid sarcoma. Immunohistochemical study. Therapy with recombinant alfa interferon].

    Medicina cutanea ibero-latino-americana·1990
    Same journal

    [Dyshidrosiform pemphigoid].

    Medicina cutanea ibero-latino-americana·1990
    Same journal

    [Metastatic alopecia].

    Medicina cutanea ibero-latino-americana·1990
    See all related articles

    Hereditary acrokeratotic poikiloderma of Weary, a rare skin condition, may present in two forms: complete (Weary type) and incomplete (Piñol type). Histological findings of keratotic lesions are detailed for the first time.

    Area of Science:

    • Dermatology
    • Medical Genetics

    Background:

    • Hereditary acrokeratotic poikiloderma of Weary is a rare genetic skin disorder.
    • Previous cases have been documented, but histological details of keratotic lesions were lacking.

    Observation:

    • A new case of hereditary acrokeratotic poikiloderma of Weary is presented.
    • The patient exhibited no eczematoid dermatitis and was the sole affected family member.
    • Clinical similarities were noted with previously reported cases by Piñol Aguadé and co-workers.

    Findings:

    • The study suggests the disease may manifest in two forms: a complete (Weary type) and an incomplete (Piñol type).
    • Histology of the keratotic lesions is reported for the first time.
    • Lesions across 15 reported cases (up to 1975) show significant similarity, supporting a distinct disease entity.

    Related Experiment Videos

    Implications:

    • This research contributes to a better understanding of the phenotypic variability of hereditary acrokeratotic poikiloderma.
    • The histological data provides a foundation for future diagnostic criteria and research into the pathogenesis of this condition.
    • Recognition of distinct clinical forms may aid in more accurate diagnosis and management of patients.