The 20 Best Andermann Syndrome Doctors Near Me in plymouth, WI

Find the Top Andermann Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Andermann Syndrome near plymouth, WI. Of these, 1 are Advanced and 1 are Experienced.

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2 providers found
    Experienced in Andermann Syndrome

    Dr. George S. Schroeder
    Family Medicine
    Experienced in Andermann Syndrome

    Dr. George S. Schroeder
    Family Medicine

    Plymouth Family Physicians S.C.

    1000 Eastern Ave, 
    Plymouth, WI 
     (0.5 miles away)
    920-893-0526
    Languages Spoken:
    English
    See accepted insurances

    George Schroeder is a primary care provider, practicing in Family Medicine in Plymouth, Wisconsin. Dr. Schroeder is rated as an Experienced provider by MediFind in the treatment of Andermann Syndrome. His clinical expertise encompasses Cirrhosis, Familial Combined Hyperlipidemia, Xanthoma, and Septic Arthritis.

    Advanced in Andermann Syndrome
    Advanced in Andermann Syndrome
    Referral may be required

    Aurora Neurology

    2414 Kohler Memorial Dr, 
    Sheboygan, WI 
     (11.9 miles away)
    920-457-4461
    Languages Spoken:
    English
    See accepted insurances
    Accepting New Patients

    Paul Guidos is a Neurologist practicing medicine in Sheboygan, Wisconsin. Dr. Guidos is rated as an Advanced provider by MediFind in the treatment of Andermann Syndrome. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Primary Orthostatic Tremor, Hereditary Sensory Neuropathy Type 1 (HSN1), Tomaculous Neuropathy, Reconstructive Urology Surgery, and Nephrectomy. Dr. Guidos is board certified in American Board Of Psychiatry & Neurology. Dr. Guidos is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Andermann Syndrome?

    Andermann syndrome (AS) is a disorder that damages the nerves used for muscle movement and sensation (motor and sensory neuropathy). Agenesis or malformation of the corpus callosum also occurs in most people with this disorder. Signs and symptoms of the disorder include areflexia; hypotonia; amyotrophy; severe progressive weakness and loss of sensation in the limbs; and tremors. Other features may include intellectual disability, seizures, contractures, scoliosis, various psychiatric symptoms, various atypical physical features, and cranial nerve problems that cause facial muscle weakness, ptosis, and difficulty following movements with the eyes (gaze palsy). It is caused by genetic changes in the SLC12A6 gene and is inherited in an autosomal recessive manner.

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