Genetic Testing for Epilepsy and Neurodevelopmental Disorders in the Pediatric Setting
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Genetic Testing for Epilepsy and Neurodevelopmental Disorders in the Pediatric Setting
A video from Ingo Helbig and Anna Prentice (as part of Dravet Syndrome Foundation), posted on Jul 15, 2025.
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Meet Ben. Ben has Angelman Syndrome which is an extremely rare genetic condition that affects around one in 15,000 children. It affects the nervous system and can cause physical and learning disabilities. The first symptoms of Angelman syndrome usually appear in children between 1 and 4 years of age. These symptoms may include: Absence or near absence of speech Developmental delays Learning disabilities Ataxia (problems with movement and balance) Epilepsy Small head size #epilepsyawareness #epil
2:09
Meet Ben. Ben has Angelman Syndrome which is an extremely rare genetic condition that affects around one in 15,000 children. It affects the nervous system and can cause physical and learning disabilities. The first symptoms of Angelman syndrome usually appear in children between 1 and 4 years of age. These symptoms may include: Absence or near absence of speech Developmental delays Learning disabilities Ataxia (problems with movement and balance) Epilepsy Small head size #epilepsyawareness #epil
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47:02
Medanta Noida’s 6 O’Clock Neuro Talk: Your monthly space to understand brain, nerve & spine health, simplified by experts. Episode 3: Fits, Fainting & Epilepsy – Doctors Decode Sudden fainting, seizures, or “fits” can be frightening — not just for patients, but for families too. Many times, people panic, delay care, or confuse one condition for another. In this session, Medanta experts come together to decode what really happens during fits, fainting episodes, and epilepsy — and when you should
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Epilepsy Treatment | Treating Seizures | Epilepsy Foundation
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Meet Ben. Ben has Angelman Syndrome which is an extremely rare genetic condition that affects around one in 15,000 children. It affects the nervous system and can cause physical and learning disabilities. The first symptoms of Angelman syndrome usually appear in children between 1 and 4 years of age. These symptoms may include: Absence or near absence of speech Developmental delays Learning disabilities Ataxia (problems with movement and balance) Epilepsy Small head size #epilepsyawareness #epil
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