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

Dominant disorders with multiple organ involvement.

M F Kegel

    Dermatologic Clinics
    |January 1, 1987
    PubMed
    Summary
    This summary is machine-generated.

    Diagnosing genetic skin disorders like incontinentia pigmenti can be challenging due to varied symptoms. Careful clinical evaluation and genetic counseling are essential for affected individuals and families.

    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

    Subungual tumors in incontinentia pigmenti.

    Archives of dermatology·1986
    Same author

    Metastasis of pulmonary carcinoma to the nail unit.

    Cutis·1985
    See all related articles

    Area of Science:

    • Dermatology
    • Clinical Genetics

    Background:

    • Incontinentia pigmenti (IP), incontinentia pigmenti achromians (IPA), and focal dermal hypoplasia (FDH) are rare genetic skin disorders.
    • These conditions present with a wide spectrum of clinical manifestations, complicating diagnosis.

    Purpose of the Study:

    • To highlight the diagnostic challenges associated with IP, IPA, and FDH.
    • To emphasize the need for precise diagnostic criteria and careful genetic counseling.

    Main Methods:

    • Review of existing literature on the clinical and genetic aspects of IP, IPA, and FDH.
    • Analysis of diagnostic criteria and genetic patterns.

    Main Results:

    • The genetic patterns of IP, IPA, and FDH are not fully elucidated.

    Related Experiment Videos

  • Existing literature can be confusing, leading to diagnostic difficulties.

    • Conclusions:

    • Strict adherence to clinical criteria is necessary for accurate diagnosis of these genodermatoses.
    • Genetic counseling for affected families requires meticulous attention and care.