LissencephalySymptoms, Doctors, Treatments, Advances & More
Lissencephaly Overview
Learn About Lissencephaly
Condition 101 content is not available at this time, but we are continually updating the site. Please check back.
However, there may be experts who have treated this or similar conditions in our Find a Doctor section and research may be available in our Latest Advances section.
Tatsushi Toda practices practicing medicine in Tokyo, Japan. Toda is rated as an Elite expert by MediFind in the treatment of Lissencephaly. They are also highly rated in 54 other conditions, according to our data. Their clinical expertise encompasses Walker-Warburg Syndrome, Fukuyama Type Muscular Dystrophy, Lissencephaly, Thrombectomy, and Bone Marrow Transplant.
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William Dobyns is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Minneapolis, Minnesota. He has been practicing medicine for over 48 years. Dr. Dobyns is rated as an Elite provider by MediFind in the treatment of Lissencephaly. He is also highly rated in 46 other conditions, according to our data. His clinical expertise encompasses Increased Head Circumference, Cerebellar Hypoplasia, Cortical Dysplasia, and Lissencephaly. Dr. Dobyns is currently accepting new patients.
Fiona Francis practices practicing medicine in Paris, France. Ms. Francis is rated as an Elite expert by MediFind in the treatment of Lissencephaly. She is also highly rated in 11 other conditions, according to our data. Her clinical expertise encompasses Lissencephaly 1, Subcortical Band Heterotopia, Miller-Dieker Syndrome, and Lissencephaly.
Summary: This is a 24-month, observational study of up to 1000 participants with Limb Girdle Muscular Dystrophy (LGMD), Myotonic Dystrophy Type 2 (DM2), and late onset Pompe disease (LOPD).
Summary: Simons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders and may be associated with autism. Simons Searchlight collects medical, behavioral, learning, and developmental information from people who have these rare genetic changes. The goal of this study is to improve the clinical care and treatment...