Events
Conferences, galas and community gatherings.
17–18 September 2026
II International Menkes Conference
An event full of purpose. Every ticket supports babies with Menkes Disease. Charity Gala to raise funds for ongoing research and patient support.
Save the Date
Charity Gala
MARCO II Benefit Evening — Every Ticket Supports the Named-Patient Programme
An evening of purpose, raising funds for the Named-Patient Programme that provides elesclomol-copper (ES-Cu) treatment to children with Menkes disease.
Free parking available
Tickets
Dinner & Party
€125
Host introduction, chef-prepared menu by Marcos Bellora with wine pairing, and art auction & quiz.
Party Only
€30
From 23:00 — soft drink, aperitif, and live music.
RSVP & Payment
Proof of payment and the names of all guests must be sent upon purchase.
Contact: vicentemateos1@hotmail.com · 651 652 699
Bank transfer: ES40 2100 0928 1302 0006 3432
Menkes International Association
MARCO II
Menkes Disease, Copper & Human Health
Under the Honorary Presidency of Her Majesty The Queen of Spain
Casa de S.M. el Rey · Credential No. 137/2026
Dates
17–18 September 2026
Venue
Centre Pompidou Málaga, Spain
Format
Hybrid: online & in-person
Languages
Spanish & English
Speakers
25 international researchers & clinicians
Fees
No fees
Accommodation
Hotel Maestranza (4★) — special rate 165 euros (breakfast included)
Contact: maestranza@mshoteles.com
Streaming Links
Day 1 – 17 September: youtube.com/live/vxsccLsoHt4Day 2 – 18 September: youtube.com/live/S9sIf2AhMiQMARCO II is the second international scientific meeting dedicated to Menkes disease, copper metabolism, and the broader landscape of rare copper-related disorders — bringing together leading researchers, clinicians, policy-makers, patient families, and philanthropic stakeholders.
Building on the success of the inaugural MARCO I meeting held in Málaga in September 2024, this two-day conference deepens the scientific dialogue around diagnosis, treatment, gene therapy, and the lived experience of those affected by rare copper diseases. Researchers will present the latest advances in copper homeostasis, novel therapeutic strategies, neonatal screening, and the intersection of policy and access.
Topics include diagnosis, treatment, gene therapy, neonatal screening, copper homeostasis, patient-centred research and healthcare policy.
Scientific Talks
Latest research on copper metabolism, Menkes disease, gene therapy, neonatal screening, and rare copper disorders from leading international institutions.
Round Tables
Multidisciplinary discussion sessions covering philanthropy, pharma innovation, health journalism, and patient-centred research.
Family Sessions
Dedicated space for families living with rare copper disorders to share testimonials and connect with the research community.
International Scope
Participants from across Europe, the Americas, and beyond — uniting science and human experience across borders.