Evidence of ongoing complement activation on adipose tissue from an 11‐year‐old girl with Barraquer

Evidence of ongoing complement activation on adipose tissue from an 11‐year‐old girl with Barraquer–Simons syndrome

Published:2020-09-05 Issue:12 Volume:47 Page:1439-1444
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Corvillo Fernando¹²^ORCID,Nozal Pilar¹²³,López‐Lera Alberto¹²,De Miguel María P.⁴,Piñero‐Fernández Juan Alberto⁵,De Lucas Raúl⁶,García‐Concepción María D⁷,Beato María J.⁷,Araújo‐Vilar David⁸,López‐Trascasa Margarita¹⁹

Affiliation:

1. Complement Research Group, Hospital La Paz Institute for Health Research (IdiPAZ) La Paz University Hospital MadridSpain

2. Center for Biomedical Network Research on Rare Diseases (CIBERER U754) MadridSpain

3. Unit of Immunology La Paz University Hospital MadridSpain

4. Cell Engineering Laboratory La Paz University Hospital Research Institute, IdiPAZ MadridSpain

5. Department of Nephrology Hospital Universitario Virgen de la Arrixaca MurciaSpain

6. Departments ofDepartment of DermatologyLa Paz University Hospital MadridMadridSpain

7. Department of Pathology La Paz University Hospital Madrid MadridSpain

8. Thyroid and Metabolic Diseases Unit (U.E.T.eM.), Centre for Research in Molecular Medicine and Chronic Diseases (CIMUS)‐IDIS, University of Santiago de Compostela School of Medicine Universidad de Santiago de Compostela Santiago de CompostelaSpain

9. Universidad Autónoma de Madrid Madrid Spain

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.15570

Reference15 articles.

1. The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline

2. An overview of lipodystrophy and the role of the complement system

3. Complement-mediated adipocyte lysis by nephritic factor sera.

4. Abnormal lipid storage related to adipocyte shrinkage in acquired partial lipodystrophy (Barraquer–Simons syndrome)

5. Adipose cell morphology and control of lipolysis in a patient with partial lipodystrophy

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