Report ID: SQMIG35A2815
Report ID:
SQMIG35A2815 |
Region:
Global |
Published Date: July, 2024
Pages:
219
|
Tables:
92 |
Figures:
67
Drivers
Increasing Heightened Occurrence of Gene Mutations
The heightened occurrence of gene mutations, particularly mutations in the SCN1A gene, significantly contributes to the onset of Dravet syndrome in children, with approximately 80-90% of cases linked to mutations in this specific gene. The market's revenue growth is anticipated to be driven by advancements in genetic testing technologies, which have markedly improved the rate of Dravet syndrome diagnosis. The use of advanced genetic testing methods, such as identifying duplications, deletions, mosaicism, and other sophisticated diagnostic approaches, has played a pivotal role in enhancing the accuracy and efficiency of detecting genetic abnormalities associated with Dravet syndrome.
Restraints
Potential Impediments
The anticipated revenue growth of Dravet syndrome faces potential impediments attributed to various factors. Historically, epilepsy and related seizure disorders have been shrouded in societal stigma, discrimination, misinformation, and fear across many regions globally. The pervasive stigma associated with the ailment could act as a deterrent for individuals seeking treatment, as the fear of being identified with such a condition may discourage them from seeking the necessary medical care.
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Report ID: SQMIG35A2815