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.
Reference: Access aggregated data from Orphanet at Orphadata.
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.
Advocacy Organizations
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.
Clinical Trials
For a list of clinical trials in this disease area, please click here.