One Rare Disease
One Global Family
Families and researchers from 29 countries united by one goal — better outcomes for every child with Menkes disease.
II International Menkes Conference
17–18 September 2026 · Charity Gala included
What is Menkes Disease?
A rare genetic disorder requiring global collaboration to overcome.
Genetic & Rare
Menkes disease is a rare X-linked recessive disorder affecting copper transport, caused by mutations in the ATP7A gene.
Affects Families
Primarily affecting male infants, it causes severe neurological deterioration. Early diagnosis is critical to improve outcomes.
Active Research
International teams are working on copper-histidine treatments and gene therapies. The MIA library tracks every breakthrough.
138
Registered patients
29
Countries represented
2020
Founded in Spain
Early Diagnosis of Menkes Disease
Free brochure by the Copper(less) Committee — for paediatricians and families
Latest News
All newsMarch 2026
New Menkes Awareness Brochure Released
The Copper(less) Committee published an updated early diagnosis brochure in English, available for free download.
February 2026
II International Menkes Conference — September 2026
The second international conference will take place 17–18 September 2026.
January 2026
Fortress Biotech Reports Positive Clinical Results
Positive topline data announced for Menkes disease treatment trials — a landmark step for the community.
Support Our Mission
Every donation goes directly to funding research, supporting families, and building the tools that will make Menkes disease history. No intermediaries, no fees — direct bank transfer to our Spanish foundation account.
Donate via Bank Transfer