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

[Iridoschisis (author's transl)]

W Lisch

    Klinische Monatsblatter Fur Augenheilkunde
    |February 1, 1976
    PubMed
    Summary
    This summary is machine-generated.

    Iridoschisis, a condition affecting the iris, presents distinct alterations. It requires differentiation from similar iris and corneal conditions due to potential genetic links.

    Related Experiment Videos

    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

    [The cornea as an indicator for systemic diseases].

    Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete·2019
    Same author

    [The cornea as an indicator for systemic diseases].

    Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft·2018
    Same author

    Recurrence of paraproteinemic keratopathy after penetrating keratoplasty and its assessment with confocal microscopy.

    American journal of ophthalmology case reports·2018
    Same author

    [Hematological diagnosis in the corneal consultation].

    Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft·2017
    Same author

    [Yellowish, prominent tumor of the corneal periphery].

    Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft·2017
    Same author

    [Paraproteinemic Keratopathy as a Clinical Sign of Monoclonal Gammopathy].

    Klinische Monatsblatter fur Augenheilkunde·2017
    Same journal

    Corneal Neurotisation in Neurotrophic Keratopathy: A Retrospective Analysis of Functional Outcomes and Clinical Courses.

    Klinische Monatsblatter fur Augenheilkunde·2026
    Same journal

    Evaluating the Long-term Success and Safety of Canaloplasty in Glaucoma Patients.

    Klinische Monatsblatter fur Augenheilkunde·2026
    Same journal

    Imbalanced Trace Elements as Risk Factors in the Pathogenesis of Glaucoma.

    Klinische Monatsblatter fur Augenheilkunde·2026
    Same journal

    Malnutrition as a Risk Factor for Cerebral and Glaucomatous Neurodegeneration - Mechanisms and Therapeutic Strategies.

    Klinische Monatsblatter fur Augenheilkunde·2026
    Same journal

    Impact of Wearing a Face Mask on the Reliability of Standard Automated Perimetry in Glaucoma Patients and Suspects: a Retrospective Longitudinal Study.

    Klinische Monatsblatter fur Augenheilkunde·2026
    Same journal

    [Siderotic Cataract Eight Months After Intralenticular Metallic Foreign Body: A Case Report and Surgical Management].

    Klinische Monatsblatter fur Augenheilkunde·2026
    See all related articles

    Area of Science:

    • Ophthalmology
    • Genetics

    Context:

    • Discusses characteristic alterations of Iridoschisis (Type I and II) based on observational data.
    • Highlights the importance of differentiating Iridoschisis from other ocular conditions.

    Purpose:

    • To present observations on Iridoschisis alterations.
    • To clarify diagnostic distinctions between Iridoschisis and related disorders.

    Summary:

    • Iridoschisis involves specific iris changes, classified into Type I and II.
    • Differential diagnosis is crucial, distinguishing it from essential progressive iris atrophy, Rieger syndrome, Chandler syndrome, and polycoria.
    • Genetic interrelationships suggest a predisposition for these conditions.

    Impact:

    • Aids in accurate diagnosis and management of Iridoschisis.
  • Informs understanding of the genetic basis and predisposition for iris and corneal anomalies.
  • Contributes to the differential diagnosis of anterior segment dysgenesis.