SCN1A-associated Episodic Encephalopathy in a School-aged Child: A Phenotypic Overlap with Familial Hemiplegic Migraine? (P10-10.009)

Lin Yao; Jeff Kuerbitz; Melissa Mizerik; M. C. González; Prescott Cheong; Rachael Cheek; Jimmy Holder; Gary Clark; Mariam Hull

doi:10.1212/wnl.0000000000216416

June 9, 2026Neurology

SCN1A-associated Episodic Encephalopathy in a School-aged Child: A Phenotypic Overlap with Familial Hemiplegic Migraine? (P10-10.009)

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Key Points

To examine the phenotypic similarities between SCN1A-associated episodic encephalopathy and familial hemiplegic migraine in a school-aged child.
Case report of a child with SCN1A mutation.
Comparative analysis of symptoms with familial hemiplegic migraine.
Notable overlap in clinical manifestations between episodic encephalopathy and familial hemiplegic migraine.
Identification of potential genetic factors influencing both conditions.

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Implication

Case report explores phenotypic overlaps in SCN1A-associated episodic encephalopathy and familial hemiplegic migraine, indicating possible genetic links.

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Cite This Study

Yao et al. (2026) studied this question.

synapsesocial.com/papers/6a2cf3d6faef96ed7f05653f https://doi.org/10.1212/wnl.0000000000216416

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SCN1A-associated Episodic Encephalopathy in a School-aged Child: A Phenotypic Overlap with Familial Hemiplegic Migraine? (P10-10.009)

Key Points

No abstract yet

Implication

Discussion

Cite This Study

SCN1A-associated Episodic Encephalopathy in a School-aged Child: A Phenotypic Overlap with Familial Hemiplegic Migraine? (P10-10.009)

Key Points

No abstract yet

Implication

Discussion

Cite This Study

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