Volume 8, Issue 11 pp. 2181-2185

CASE REPORT

Open Access

Endocrinopathies in Aicardi Goutières syndrome—A descriptive case series

Chris Worth,

Corresponding Author

Chris Worth

[email protected]

orcid.org/0000-0001-6609-2735

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK

Correspondence

Chris Worth, Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, UK.

Email: [email protected]

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Tracy A Briggs,

Tracy A Briggs

Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester Academic Health Sciences Centre, Manchester University Hospitals NHS Foundation Trust, Manchester, UK

Division of Evolution and Genomic Sciences, School of Biological Sciences, University of Manchester, Manchester, UK

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Raja Padidela,

Raja Padidela

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK

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Eleanor Balmer,

Eleanor Balmer

Department of Paediatrics, Royal Manchester Children's Hospital, Manchester, UK

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Mars Skae,

Mars Skae

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK

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Chris Worth,

Corresponding Author

Chris Worth

[email protected]

orcid.org/0000-0001-6609-2735

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK

Correspondence

Chris Worth, Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, UK.

Email: [email protected]

Search for more papers by this author

Tracy A Briggs,

Tracy A Briggs

Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester Academic Health Sciences Centre, Manchester University Hospitals NHS Foundation Trust, Manchester, UK

Division of Evolution and Genomic Sciences, School of Biological Sciences, University of Manchester, Manchester, UK

Search for more papers by this author

Raja Padidela,

Raja Padidela

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK

Search for more papers by this author

Eleanor Balmer,

Eleanor Balmer

Department of Paediatrics, Royal Manchester Children's Hospital, Manchester, UK

Search for more papers by this author

Mars Skae,

Mars Skae

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK

Search for more papers by this author

First published: 23 July 2020

https://doi.org/10.1002/ccr3.3081

Citations: 3

Funding information

TAB is funded by the Medical Research Foundation.

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Abstract

Hypothyroidism and diabetes insipidus present in children with Aicardi Goutières Syndrome (AGS) often years after disease onset and frequently resolve spontaneously. Screening and regular reassessment for both conditions are recommended in all children with AGS.

CONFLICT OF INTEREST

We report no conflict of interest.

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Volume8, Issue11

November 2020

Pages 2181-2185

Endocrinopathies in Aicardi Goutières syndrome—A descriptive case series

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Endocrinopathies in Aicardi Goutières syndrome—A descriptive case series

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