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Interview of Prof. David Araújo-Vilar in La Voz de Galicia

20 Oct, 2019
La Voz de Galicia (Press article)


The experience of Yolanda Pérez

31 Mar, 2019
«We need resources to investigate, both in Santiago and in the Hospital of La Paz to see if we can eradicate this disease.»

La Voz de Galicia (Press article)

Experience in the treatment and importance of the lipodystrophy approach

26 Mar, 2019

Importance of the early diagnostic and information to patients


Diariomedico (Press article)

How to diagnose a rare disease for the first time: "The worst that can happen to you"

28 Feb, 2019

The name Celia's Encephalopathy is a tribute to Celia's memory and was chosen in agreement with her parents, to whom we are deeply indebted for their collaboration and commitment to research.



El Confidencial (Press article)

"Galicia, holy grail of rare diseases"

28 Feb, 2019

Francisco, patient of Dr. David Araújo-Vilar, has an atypical progeroid syndrome that presents with a generalized lipodystrophy.



La Voz de Galicia (Press article)

Samy Basso, the young scientist working hand in hand with Carlos López-Otín to look for a cure for his "lightning aging"

18 Feb, 2019

El joven científico Sammy Basso busca una cura para su 'envejecimiento relámpago'


Sammy Basso, Carlos López-Otín and the research group

El Mundo (Press article)

Link to the the research article in Nature Medicine

"Leticia, the only living case"

4 Mar, 2018

La Opinión de Murcia (press article)

"87,000 families in the region of Murcia are affected by rare diseases"

28 Feb, 2018

Cadena Ser (press article)

"The Galician miracle of Leticia"

26 Jan, 2018

La Voz de Galicia (press article)


"Five years waiting for a diagnosis"

14 Oct, 2016
La Voz de Galicia (press article)


"Prof. David Araújo-Vilar participates in a global study of lipodystrophy"

14 Oct, 2016
El Faro de Vigo (press article)


"Genetics and decades of research confront a rare disease in the region of Murcia"

25 Jun, 2016
Europa Press (press article)

"The Celia's Encephalopathy, the degenerative syndrome with six cases all over the world"

7 Jun, 2016
Público (press article)

"Celia, the girl who gave name to a disease with only 6 cases in the world"

6 Jun, 2016
BBC (press article)

"In search of the Celia's gene"

1 May, 2016
La Verdad (press article)

"The rare disease 'hidden' in the region of Murcia"

26 Apr, 2016
El Mundo (press article)

"A lipodystrophy from the cradle"

31 Mar, 2016
La Vanguardia (press article)

AELIP president: "We must go on in a network to overcome rare diseases"

13 Mar, 2016
La Voz de Galicia (press article)

"The only case in the world of a rare disease is being treated in Santiago de Compostela"

9 Mar, 2016
La Voz de Galicia (press article)

"157 lipodystrophic patients from various countries are being treated in Santiago de Compostela"

31 Mar, 2015

La Voz de Galicia (press article)

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Recent Posts

  • 2023 ECLip Annual Meeting SAVE THE DATE!!!
    1 Jun, 2022
  • A Novel, Heterozygous BSCL2 Variant in Association With Early-Onset Epileptic Encephalopathy
    14 May, 2022
  • Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)
    14 May, 2022
  • Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real-life experience from a national reference network
    14 May, 2022
  • Metreleptin for the treatment of lipodystrophy: leading the way among novel therapeutics for this unmet clinical need
    14 May, 2022
  • Seipin forms a flexible cage at lipid droplet formation sites
    14 May, 2022
  • Clinical Effects of Sodium-Glucose Transporter Type 2 Inhibitors in Patients With Partial Lipodystrophy
    14 May, 2022
2019 UETeM Laboratory