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1
Introduction
2
History
3
Clinical Disorders
4
Epilepsy
5
Epilepsy as a Presenting Symptom
6
Developmental Plateauing
7
Progressive Vision Impairment
8
Seizures
9
Diagnosis
10
Multidisciplinary Care
11
Family Trauma Loss Framework
12
Research Grant Program
13
Product Projects
14
Diagnostic Footprint
15
Focus on Early Diagnosis
16
Family Photos
17
Center of Excellence
18
Batten Siblings
19
Lance Johnston
20
Research Team
21
Language Delay
22
Clinical Trials
23
Gene Therapy
24
Treatment Trials
25
Upcoming Trials
26
Genetic Testing
27
QA
Description:
Explore epilepsy as a presenting feature of Batten disease in this informative 58-minute webinar presented by Ambry Genetics. Gain insights from doctors Margie Frazier and Kaleb Yohay as they delve into the history, clinical disorders, and diagnostic processes associated with this rare genetic condition. Discover the importance of early diagnosis, multidisciplinary care, and the latest research developments, including gene therapy and clinical trials. Learn about the Batten Disease Support and Research Association's initiatives, including their research grant program and focus on supporting affected families. Understand the challenges faced by Batten siblings and the role of genetic testing in diagnosis. Engage with a comprehensive overview of this complex neurological disorder, from its initial epilepsy symptoms to the progressive vision impairment and developmental plateauing characteristic of the disease.

Epilepsy as a Presenting Feature of Batten Disease - Webinar - Ambry Genetics

Ambry Genetics
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