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FEDERG in 53rd Congress of the Spanish Society of Nephrology 2023.FEDERG in

Homepage Education FEDERG in 53rd Congress of the Spanish Society of Nephrology 2023.FEDERG in

FEDERG in 53rd Congress of the Spanish Society of Nephrology 2023.FEDERG in

Susana Carvajal Arjona
11 November 2023
Education, Rare Disease

From November 11 to 13, Palau de Congresos Palma de Mallorca 2023.

Within the framework of the 53rd Congress of the Spanish Society of Nephrology, Federg had the opportunity to disseminate the federation of European groups with rare and genetic diseases. AIRG Spain, Alcer and Hipofam were present and were able to attend the advances in nephrology with the help of experts. Innovations and results on the number of patients who undergo kidney transplant without a diagnosed cause, innovations in the treatment of patients with Shua, were of interest to our members. Likewise, with the help of Juan Carlos Julián and Dani Gallego and Antonio Cabrera representing ALCER, the studies of the childhood and adolescence group, Recommendations of patients for the Transition towards adolescence of patients with CKD, were presented.

Likewise, ARIG Spain with its president Marta Roger and Antonio Cabrera participated in the SEN  hereditary kidney diseases working group. GTERH.The SEN offered FEDERG members the booth with free charges and sufficient support to our members to facilitate their presence and learning in the different presentations presented during 3 days.

Antonio Cabrera (Alcer/hipofam, AIRG) Juan Carlos Julián (Federg, Alcer, EKPF) Susana Carvajal Arjona (FEDERG) Marta Roger (AIRG) Dani Gallego (Alcer, EKPF)

Tags: EURORDIS HIPOFAM Rare Disease
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About Us

FEDERG is the non-profit federation of European associations of patients affected by rare and/or genetic kidney diseases.

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  • Alport Syndrome Patient Information Day on September 6th, 2026! Wednesday, 14, Jan
  • AIRG, 21st Annual Meeting in Madrid, January 17, 2026 Sunday, 11, Jan
  • Members activities Newsletter, volume 2. Tuesday, 16, Sep

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Wednesday, 14, Jan
Alport Syndrome Patient Information Day on September 6th, 2026!
Sunday, 11, Jan
AIRG, 21st Annual Meeting in Madrid, January 17, 2026
Tuesday, 16, Sep
Members activities Newsletter, volume 2.
Tuesday, 16, Sep
FEDERG support the adoption of the WHA Resolution on Rare Diseases.
Monday, 9, Jun
FEDERG strongly support the WHA Resolution on rare Diseases
Thursday, 19, Sep
Fighting for our federation Federg f2f Members meeting September 14 Martorell