The 20 Best Landau-Kleffner Syndrome Doctors Near Me in parsons, WV

Find the Top Landau-Kleffner Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Landau-Kleffner Syndrome near parsons, WV. Of these, 2 are Experienced.

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2 providers found
    Experienced in Landau-Kleffner Syndrome
    Family Medicine
    Experienced in Landau-Kleffner Syndrome
    Family Medicine

    Belington Community Medical Services Association

    70 N Sturmer St, 
    Belington, WV 
     (14.6 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Hannah Valentine is a primary care provider, practicing in Family Medicine in Belington, West Virginia. Dr. Valentine is rated as an Experienced provider by MediFind in the treatment of Landau-Kleffner Syndrome. Her clinical expertise encompasses Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, Hypertension, and Maturity Onset Diabetes of the Young. Dr. Valentine is currently accepting new patients.

    Experienced in Landau-Kleffner Syndrome
    Family Medicine
    Experienced in Landau-Kleffner Syndrome
    Family Medicine

    Davis Medical Center

    812 Gorman Ave, 
    Elkins, WV 
     (14.9 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Johanna Biola is a primary care provider, practicing in Family Medicine in Elkins, West Virginia. Dr. Biola is rated as an Experienced provider by MediFind in the treatment of Landau-Kleffner Syndrome. She is also highly rated in 15 other conditions, according to our data. Her clinical expertise encompasses Vitamin B12 Deficiency, Chronic Obstructive Pulmonary Disease (COPD), Plantar Fasciitis, and Lung Metastases. Dr. Biola is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Landau-Kleffner Syndrome?

    Landau-Kleffner syndrome (LKS) is a rare neurological syndrome characterized by the sudden or gradual development of aphasia (the inability to understand or express language) and recurrent seizures (epilepsy). Males are more often affected by LKS than females. In about 20% of people with LKS, genetic changes (changes) in the GRIN2A gene have been identified. The syndrome is inherited in an autosomal dominant manner. In other cases, the syndrome may be caused by changes to other unidentified genes. LKS is diagnosed when a doctor sees clinical features that are consistent with the syndrome such as a loss of speech and an electroencephalogram (EEG) that shows specific kinds of seizure activity. Genetic testing can be used to confirm if there is a genetic change in GRIN2A, but this testing is not done routinely.

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