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

Myotonic dystrophy associated with thyroid disease.

E Rioperez, J M Botella, A Palacio

    Journal of the Neurological Sciences
    |November 1, 1979
    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

    The view of experts on initiatives to be undertaken to promote equity in the access to orphan drugs and specialised care for rare diseases in Spain: A Delphi consensus.

    Health policy (Amsterdam, Netherlands)·2018
    Same author

    Fistula from circumflex coronary artery to superior vena cava.

    Circulation·2015
    Same author

    Identifying data sources for a national population-based registry: the experience of the Spanish Rare Diseases Registry.

    Public health·2015
    Same author

    Childhood vasculitis hospitalizations in Spain, 1997-2011.

    Georgian medical news·2014
    Same author

    Prevalence of dystrophic epidermolysis bullosa in Spain: a population-based study using the 3-source capture-recapture method. Evidence of a need for improvement in care.

    Actas dermo-sifiliograficas·2013
    Same author

    Reference centers for epidermolysis bullosa and ichthyosis: an urgent need in Spain.

    Actas dermo-sifiliograficas·2013
    Same journal

    Distinguishing drug-target effects from natural lipid variation and incorporating imaging outcomes in Mendelian randomisation studies of multiple sclerosis.

    Journal of the neurological sciences·2026
    Same journal

    Long-term social cognitive impairment after ischemic stroke: Frequency and association with lesion volume and location in an exploratory pilot study.

    Journal of the neurological sciences·2026
    Same journal

    Subjective cognitive decline among U.S. Cancer survivors, 2017-2024: Prevalence, cancer-specific patterns, and associated factors.

    Journal of the neurological sciences·2026
    Same journal

    Comment on "Comparative impact of mental and cardiovascular comorbidities on adverse outcomes in people with MS".

    Journal of the neurological sciences·2026
    Same journal

    Comment on "Efficacy and safety of conventional immunosuppressant therapies in elderly patients with Neuromyelitis optica spectrum disorder: A target trial emulation study".

    Journal of the neurological sciences·2026
    Same journal

    Increasing incidence of varicella-zoster virus meningitis in Japan, 2011-2022.

    Journal of the neurological sciences·2026
    See all related articles

    This study examines two myotonic dystrophy patients with co-occurring thyroid disorders, including hypothyroidism and goiter. The findings highlight potential links between these distinct conditions and their muscle/metabolic effects.

    Area of Science:

    • Neurology
    • Endocrinology
    • Genetics

    Background:

    • Myotonic dystrophy is a hereditary neuromuscular disorder.
    • Thyroid disorders, such as hypothyroidism and goiter, affect metabolic processes.
    • The co-occurrence of myotonic dystrophy and thyroid disease is rare.

    Observation:

    • Two patients presenting with classic myotonic dystrophy also exhibited thyroid abnormalities.
    • One patient had primary hypothyroidism, while the other had a non-toxic multinodular goiter requiring surgery.
    • Electromyography (EMG) and muscle histopathology were analyzed in both patients.

    Findings:

    • Muscle and metabolic changes in the patients were evaluated in the context of both myotonic dystrophy and hypothyroidism.
    • The study compared the observed EMG and histopathological findings with those typically seen in hypothyroidism.

    Related Experiment Videos

  • The genetic basis for the simultaneous occurrence of these two conditions remains unclear.

    • Implications:

    • The findings suggest a potential, though unexplained, association between myotonic dystrophy and thyroid disorders.
    • Further research is needed to understand the underlying mechanisms connecting these conditions.
    • This case series contributes to the limited literature on the dual diagnosis of myotonic dystrophy and thyroid disease.