Alternating hemiplegia of childhood

Get in touch with RARE Concierge.

Contact RARE Concierge

Synonyms: AHC

A rare genetic neurodevelopmental disorder characterized by early-onset of recurrent transient episodes of hemiplegia (including quadriplegia) which typically disappear upon sleep.

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 May 2024

Newly diagnosed with
Alternating hemiplegia of childhood?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

Alternating Hamiplegia of Childhood Foundation

Through research, education and family support, we have ONE MISSION: END AHC We strive to find the cause(s) of AHC, develop effective treatments and ultimately find a cure, while providing support to the families and children with AHC by funding research to accomplish these goals. We promote proper diagnosis, educate health care professionals, and encourage worldwide exchange of information.

Don't see your organization here. Let us know here.

Clinical Trials

For a list of clinical trials in this disease area, please click here.