When Hemiplegic Migraine Defies Expectations: Diagnostic Complexity in a Rare Genetic Disorder
Amandine Goossens1, Ann-Laurence Delabie1, Tanguy Demaret2
1Department of Neurology, Centre Hospitalier Universitaire Tivoli, Université libre de Bruxelles (ULB), La Louvière, Belgium.
Introduction:
Familial hemiplegic migraine (FHM) is a rare and complex inherited subtype of migraine with aura, characterised by migraine with a reversible motor aura, and may present with a wide spectrum of neurological symptoms, making diagnosis particularly challenging.
Case Presentation:
We report a case of FHM presenting with prolonged hemiparesis, severe headache, altered consciousness, and fever. This constellation of symptoms initially suggested acute stroke, encephalitis, or status epilepticus. A precise clinical history and targeted genetic testing (CACNA1A, ATP1A2, SCN1A, and PRRT2) proved essential for establishing the diagnosis.
Conclusion:
This case highlights the wide phenotypic variability of FHM and the risk of misdiagnosis in emergency settings. Early recognition through careful clinical assessment and appropriate genetic testing enabled appropriate management and avoided unnecessary interventions.
Insights
Familial hemiplegic migraine (FHM) can present with diverse neurological symptoms, mimicking other serious conditions. Accurate diagnosis relies on detailed clinical history and genetic testing to ensure proper management.
Area of Science:
- Neurology
- Genetics
Background:
- Familial hemiplegic migraine (FHM) is a rare inherited migraine subtype with aura.
- FHM is characterized by reversible motor aura and a broad range of neurological symptoms, complicating diagnosis.
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