Endocrinopathies in Aicardi Goutières syndrome-A descriptive case series.
adolescent medicine
endocrinology and metabolic disorders
genetics
pediatrics
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Nov 2020
Nov 2020
Historique:
received:
03
01
2020
revised:
28
04
2020
accepted:
06
06
2020
entrez:
25
11
2020
pubmed:
26
11
2020
medline:
26
11
2020
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 33235754
doi: 10.1002/ccr3.3081
pii: CCR33081
pmc: PMC7669429
doi:
Types de publication
Case Reports
Langues
eng
Pagination
2181-2185Informations de copyright
© 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
We report no conflict of interest.
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