Endocrinopathies in Aicardi Goutières syndrome—A descriptive case series

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. Hypothyroidism and diabetes insipidus...

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Veröffentlicht in:	Clinical case reports 2020-11, Vol.8 (11), p.2181-2185
Hauptverfasser:	Worth, Chris, Briggs, Tracy A, Padidela, Raja, Balmer, Eleanor, Skae, Mars
Format:	Artikel
Sprache:	eng
Schlagworte:	adolescent medicine Age Calcification Case Report Case Reports Congenital diseases Cytomegalovirus Diabetes endocrinology and metabolic disorders Genes genetics Hypothyroidism Infections Magnetic resonance imaging Patients pediatrics Thrombocytopenia Thyroid gland Ultrasonic imaging Urine
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Zusammenfassung:	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. 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.
ISSN:	2050-0904 2050-0904
DOI:	10.1002/ccr3.3081