Unverricht-Lundborg Syndrome
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Unverricht-Lundborg Syndrome Overview

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Learn About Unverricht-Lundborg Syndrome

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.

Who are the top Unverricht-Lundborg Syndrome Local Doctors?
Elite in Unverricht-Lundborg Syndrome
Elite in Unverricht-Lundborg Syndrome
Box 100, KYS, 
Kuopio, FI 

Reetta Kalviainen practices practicing medicine in Kuopio, Finland. Kalviainen is rated as an Elite expert by MediFind in the treatment of Unverricht-Lundborg Syndrome. They are also highly rated in 14 other conditions, according to our data. Their clinical expertise encompasses Unverricht-Lundborg Syndrome, Dentatorubral-Pallidoluysian Atrophy, Lafora Disease, and Myoclonic Epilepsy.

Elite in Unverricht-Lundborg Syndrome
Elite in Unverricht-Lundborg Syndrome
P.O. Box 100, FI-70029 KYS, 
Kuopio, FI 

Ritva Vanninen practices practicing medicine in Kuopio, Finland. Vanninen is rated as an Elite expert by MediFind in the treatment of Unverricht-Lundborg Syndrome. They are also highly rated in 14 other conditions, according to our data. Their clinical expertise encompasses Unverricht-Lundborg Syndrome, Dentatorubral-Pallidoluysian Atrophy, Lafora Disease, Thrombectomy, and Mastectomy.

 
 
 
 
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Elite in Unverricht-Lundborg Syndrome
Elite in Unverricht-Lundborg Syndrome
P.O. Box 100, FI-70029 KYS, 
Box, FI 

Paivi Koskenkorva practices practicing medicine in Box, Finland. Koskenkorva is rated as an Elite expert by MediFind in the treatment of Unverricht-Lundborg Syndrome. They are also highly rated in 7 other conditions, according to our data. Their clinical expertise encompasses Unverricht-Lundborg Syndrome, Dentatorubral-Pallidoluysian Atrophy, Lafora Disease, and Myoclonic Epilepsy.

What are the latest Unverricht-Lundborg Syndrome Clinical Trials?
Registry and Natural History Study for Progressive Myoclonus Epilepsy Type 1 (EPM1)

Summary: The Registry and Natural History Study for Progressive Myoclonus Epilepsy Type 1 (EPM1) is focused on gathering longitudinal clinical data as well as biological samples (blood and/or urine) from male and female patients, of all ages, who have a molecular diagnosis of EPM1or CSTB-null-related disease. Currently, there are no therapies that halt disease progression in any CSTB-related diseases, high...

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