LAS VEGAS, April 6, 2021 /PRNewswire/ -- The Dup15q syndrome has received little attention because of its rarity, the relatively nonspecific phenotype, the clinical heterogeneity, and the broad ...
"Dup15q Syndrome Market"Dup15q syndrome is a neurogenetic condition caused by duplications on chromosome 15q11.2-13.1. It is marked by hypotonia, developmental delays, intellectual disability (ID), ...
A four-year-old girl who doctors said would never walk has defied the odds and taken her first steps. Scottie Mae Blair was diagnosed with Angelman syndrome at 11 months old. The rare genetic ...
Results from signal-finding, pilot Phase 2 open-label ARCADE study and ENDYMION long-term extension study in CDKL5 deficiency disorder (CDD) and Dup15q syndrome (Dup15q) show seizure frequency ...
“I celebrate her,” heartwarmingly shares Mom Jacqueline Vanderhoof this World Autism Awareness Day on April 2 about the amazing difference her daughter Fiona, 4, is already making in the world to ...
Soticlestat continues to appear to be safe and well-tolerated; the majority of the 11 patients showed a reduction in seizures All patients that have completed the Phase 2 ARCADE study to date have ...
Research supported by the Eagles Autism Foundation is focused on a girl in Montgomery County with the hopes of eventually finding new treatments for autism. Four-year-old Fiona Vanderhoof, who enjoys ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback