The 20 Best Lissencephaly 2 Doctors in North Korea

Find the Top Lissencephaly 2 Experts and Specialists

Last Updated: 06/30/2026

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MediFind found 2 doctor with experience in Lissencephaly 2 near North Korea. Of these, 1 are Advanced and 1 are Experienced.

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2 providers found
    Advanced in Lissencephaly 2

    Eun B. Lee
    Advanced in Lissencephaly 2

    Eun B. Lee
    Referral may be required
    Seoul, KR 

    Eun Lee practices practicing medicine in Seoul, Republic of Korea. Ms. Lee is rated as an Advanced expert by MediFind in the treatment of Lissencephaly 2. She is also highly rated in 22 other conditions, according to our data. Her clinical expertise encompasses Rheumatoid Arthritis (RA), Arthritis, Behcet Disease, and Shingles.

    Experienced in Lissencephaly 2

    Jin K. Park
    Experienced in Lissencephaly 2

    Jin K. Park
    Referral may be required
    Seoul, KR 

    Jin Park practices practicing medicine in Seoul, Republic of Korea. Park is rated as an Experienced expert by MediFind in the treatment of Lissencephaly 2. They are also highly rated in 17 other conditions, according to our data. Their clinical expertise encompasses Myositis, Rheumatoid Arthritis (RA), Arthritis, and Vasculitis.

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    Lissencephaly

    While we make every effort to provide the best results possible, data is currently limited outside of the United States. Doctors listed may include both clinicians and researchers, and individuals relocate frequently. We recommend contacting doctors directly to confirm their location and areas of focus. Contact information is provided when available. Learn more about our expert tiers.
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    Last Updated: 06/30/2026

    What is the definition of Lissencephaly 2?

    Lissencephaly 2 is an inherited condition characterized by classical lissencephaly in association with certain abnormalities of the skull and facial (craniofacial) region, such as a low, sloping forehead; abnormal prominence of the back portion of the head (occiput); a broad, prominent nasal bridge; and widely set eyes (ocular hypertelorism). Additional symptoms and findings typically include severe or profound intellectual disability, seizures, abnormally increased muscle tone (hypertonia), exaggerated reflexes (hyperreflexia), and severe growth failure. This condition is inherited in an autosomal recessive fashion. Genetic changes in the RELN gene have been identified in some affected individuals.