Primary hyperaldosteronism-seizures-neurological abnormalities syndrome
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).
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version December 2023
Newly diagnosed with
Primary hyperaldosteronism-seizures-neurological abnormalities syndrome?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Adrenal Alternatives Foundation
Advocacy & Access for all cortisol care.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
For a list of clinical trials in this disease area, please click here.