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Primary hyperaldosteronism-seizures-neurological abnormalities syndrome

ORPHA:369929· ICD-10 E26.0

Definition

A rare, genetic, neurologic disease characterized by primary hyperaldosteronism presenting with early-onset, severe hypertension, hypokalemia and neurological manifestations (including seizures, severe hypotonia, spasticity, cerebral palsy and profound developmental delay/intellectual disability).

Prevalence
<1 / 1 000 000
Inheritance
Not applicable
Age of onset
Infancy, Neonatal