Waterhouse-Friderichsen Syndrome and Central Diabetes Insipidus Due to
Escherichia coli
Waterhouse-Friderichsen syndrome
central diabetes insipidus
neonatal meningitis
ultrasound
Journal
JCEM case reports
ISSN: 2755-1520
Titre abrégé: JCEM Case Rep
Pays: England
ID NLM: 9918609886906676
Informations de publication
Date de publication:
Jan 2023
Jan 2023
Historique:
received:
19
08
2022
medline:
1
11
2023
pubmed:
1
11
2023
entrez:
1
11
2023
Statut:
epublish
Résumé
Waterhouse-Friderichsen syndrome and central diabetes insipidus are uncommon but potentially fatal endocrine and metabolic diseases. Waterhouse-Friderichsen syndrome is defined as adrenal insufficiency caused by adrenal hemorrhage, which is typically bilateral and most frequently due to meningococcal infection. It is usually diagnosed by necropsy. Central diabetes insipidus in children is often caused by trauma, intracranial lesions, autoimmune diseases, and infections. In addition, it can be caused by mutations in the AVP-NPII gene, although this occurs typically later in childhood rather than in the neonatal period. This report describes a term infant who developed
Identifiants
pubmed: 37908241
doi: 10.1210/jcemcr/luac031
pii: luac031
pmc: PMC10578388
doi:
Types de publication
Case Reports
Langues
eng
Pagination
luac031Informations de copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society.
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