Mills syndrome

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A rare acquired motor neuron disease characterized by a slowly progressive unilateral ascending or descending hemiplegia associated to unilateral or asymmetrical pyramidal signs and no sensory loss. It is a diagnosis of exclusion and controversy exists regarding whether the presence of bulbar symptoms sphincter disturbances fasciculations or cognitive manifestations characterize the disease.

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 April 2026

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Mills syndrome?

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Advocacy Organizations

Association Aux Pas du Coeur – Côte d’ivoire

Our organization wants to raise awareness and recognition of rare diseases in Ivory Coast. Our mission is to: Raise awareness and campaign to help with the diagnosis and free therapeutic care of patients. Request and/or contribute to actions relating to the training of the medical profession to be able to make a final diagnosis and ensure continuous monitoring of patients easily.

patriot for growth and development initiative

Mission: Patriots for Growth and Development Initiative (PGDI) is dedicated to fostering sustainable development, promoting peacebuilding, and empowering marginalized communities. Through innovative programs, advocacy, and partnerships, we aim to create inclusive solutions that address conflict, enhance social justice, and uplift vulnerable populations.

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Clinical Trials

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