The 20 Best Koolen De Vries Syndrome Doctors Near Me in hudson, WI

Find the Top Koolen De Vries Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 4 doctor with experience in Koolen De Vries Syndrome near hudson, WI. Of these, 4 are Experienced.

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4 providers found
    Experienced in Koolen De Vries Syndrome
    Experienced in Koolen De Vries Syndrome
    Referral may be required

    Hudson Sleep & Cpap

    2651 Hillcrest Dr, 
    Hudson, WI 
     (3.1 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Elizabeth Schertz is a Pediatrics provider practicing medicine in Hudson, Wisconsin. Dr. Schertz is rated as an Experienced provider by MediFind in the treatment of Koolen De Vries Syndrome. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Respiratory Syncytial Virus (RSV) Infection, Croup, Sleepwalking (Somnambulism), and Autism Spectrum Disorder. Dr. Schertz is currently accepting new patients.

    Experienced in Koolen De Vries Syndrome
    Experienced in Koolen De Vries Syndrome
    Referral may be required

    Office

    2651 Hillcrest Dr Ste 104, 
    Hudson, WI 
     (3.1 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Jeffrey Lynch is a Pediatrics provider practicing medicine in Hudson, Wisconsin. Dr. Lynch is rated as an Experienced provider by MediFind in the treatment of Koolen De Vries Syndrome. His clinical expertise encompasses Microcephaly Deafness Syndrome, Early Infantile Epileptic Encephalopathy, Wildervanck Syndrome, and CHARGE Syndrome. Dr. Lynch is currently accepting new patients.

    Experienced in Koolen De Vries Syndrome
    Pediatric Neurology
    Experienced in Koolen De Vries Syndrome
    Pediatric Neurology
    Referral may be required

    M Health Fairview Pediatric Specialty Clinic Woodbury

    9680 Tamarack Road, Suite 130, 
    Woodbury, MN 
     (7.8 miles away)
    Languages Spoken:
    English, Spanish
    Accepting New Patients

    Laura Speltz is a Pediatric Neurologist practicing medicine in Woodbury, Minnesota. Dr. Speltz is rated as an Experienced provider by MediFind in the treatment of Koolen De Vries Syndrome. Her clinical expertise encompasses Seizures, Generalized Tonic-Clonic Seizure, Genetic Epilepsy with Febrile Seizures Plus (GEFS+), and Epilepsy in Children. Dr. Speltz is board certified in Epilepsy: American Board Of Psychiatry And Neurology, 2018. Dr. Speltz is currently accepting new patients.

    Learn about our expert tiers
    Experienced in Koolen De Vries Syndrome
    Experienced in Koolen De Vries Syndrome
    Referral may be required

    M. Health Fairview Pediatric Therapy Woodbury

    9680 Tamarack Rd Ste 130, 
    Woodbury, MN 
     (9.7 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Teri Miller is a Pediatrics provider practicing medicine in Woodbury, Minnesota. Dr. Miller is rated as an Experienced provider by MediFind in the treatment of Koolen De Vries Syndrome. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Wildervanck Syndrome, Early Infantile Epileptic Encephalopathy, and CHARGE Syndrome. Dr. Miller is currently accepting new patients.

    Showing 1-4 of 4

    Last Updated: 09/26/2026

    What is the definition of Koolen De Vries Syndrome?

    Koolen de Vries syndrome is a disorder characterized by developmental delay, mild to moderate intellectual disability, congenital malformations, and behavioral features. Other problems include weak muscle tone (hypotonia) in childhood, recurrent seizures (epilepsy), and distinctive facial features. Males with Koolen de Vries syndrome often have undescended testes (cryptorchidism). Other symptoms may include defects in the walls between the chambers of the heart (septal defects) or other heart defects, kidney problems, and skeletal anomalies such as foot deformities. It is caused by genetic changes in the KANSL1 gene, or by the loss of a small amount of genetic material in chromosome 17 that includes the KANSL1 gene (chromosome 17 q21.31 microdeletion). Inheritance is autosomal dominant.

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