Chromosome 11 Uniparental Disomy Overview

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Learn About Chromosome 11 Uniparental Disomy

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 Chromosome 11 Uniparental Disomy Local Doctors?
Elite in Chromosome 11 Uniparental Disomy
Elite in Chromosome 11 Uniparental Disomy
Aachen, NW, DE 

Thomas Eggermann practices in Aachen, Germany. Mr. Eggermann is rated as an Elite expert by MediFind in the treatment of Chromosome 11 Uniparental Disomy. His top areas of expertise are Russell-Silver Dwarfism, Beckwith-Wiedemann Syndrome, Macroglossia, and Chromosome 11 Uniparental Disomy.

Advanced in Chromosome 11 Uniparental Disomy
Advanced in Chromosome 11 Uniparental Disomy

ETSU Physicians & Associates- Pediatrics

325 N State Of Franklin Rd, 
Johnson City, TN 
Languages Spoken:
English

. Dr. Russi is rated as an Advanced provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. His top areas of expertise are Increased Head Circumference, Ehlers-Danlos Syndrome (EDS), Chromosome 8p Deletion, and Chromosome 6q Duplication.

 
 
 
 
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Syed S. Hyder
Experienced in Chromosome 11 Uniparental Disomy
Experienced in Chromosome 11 Uniparental Disomy

Ballad Health Medical Associates Neurology

1406 Tusculum Boulevard, Suite 1200, 
Greeneville, TN 
Languages Spoken:
English
Offers Telehealth

. Dr. Hyder is rated as an Experienced provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. His top areas of expertise are Generalized Tonic-Clonic Seizure, Seizures, Parkinson's Disease, and Movement Disorders.

What are the latest Chromosome 11 Uniparental Disomy Clinical Trials?
Coordination of Rare Diseases at Sanford

Summary: CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, in...

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