Association of Adult-Onset Bartter Syndrome With Undifferentiated Connective Tissue Disorder.
bartter syndrome
hypochloremic metabolic acidosis
hypokalemia
juxta glomerular hyperplasia (jg hyperplasia)
undifferentitated connective tissue disorder (uctd)
Journal
Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737
Informations de publication
Date de publication:
Aug 2021
Aug 2021
Historique:
accepted:
12
08
2021
entrez:
17
9
2021
pubmed:
18
9
2021
medline:
18
9
2021
Statut:
epublish
Résumé
Bartter syndrome is a rare autosomal recessive, salt-losing disorder characterized by hypokalemic hypochloremic metabolic alkalosis. We are reporting a case of 21 years old patient, who presented with lower limb weakness, marked hypokalemia, proteinuria, and renal impairment detected on laboratory evaluation. The diagnosis of Bartter syndrome was suspected by marked hypokalemia and was supported by renal biopsy which showed evidence of Juxtaglomerular (JG) hyperplasia. This is the first case report about clinicopathological features of the patient with acquired Bartter syndrome and associated undifferentiated connective tissue disorder manifesting as hypokalemia with paralysis.
Identifiants
pubmed: 34532176
doi: 10.7759/cureus.17140
pmc: PMC8435068
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e17140Informations de copyright
Copyright © 2021, Saleem et al.
Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
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