Persistent Flaccid Paralysis in a Patient with Bartter Syndrome
Klin Padiatr
.
2023 Sep;235(5):299-301.
doi: 10.1055/a-1829-6365.
Epub 2023 Feb 27.
Authors
Vlasta Krejcova
1
,
Jan David
1
,
Adam Svepes
2
,
Irena Buksakowska
3
,
Eva Kantorova
4
,
Zuzana Liba
5
,
Lukas Paulas
5
,
Jana Indrakova
6
,
Jakub Zieg
1
Affiliations
1
Department of Pediatrics, Motol University Hospital, Praha, Czech Republic.
2
Department of Pediatrics, Regional hospital Ceske Budejovice, Ceske Budejovice, Czech Republic.
3
Department of Radiology, Motol University Hospital, Praha, Czech Republic.
4
Department of Medical Genetics, Regional hospital Ceske Budejovice, Ceske Budejovice, Czech Republic.
5
Department of Pediatric Neurology, Motol University Hospital, Praha, Czech Republic.
6
Department of Medical Genetics, University Hospital Ostrava, Ostrava, Czech Republic.
PMID:
36848940
DOI:
10.1055/a-1829-6365
No abstract available
MeSH terms
Bartter Syndrome* / complications
Bartter Syndrome* / diagnosis
Humans
Muscle Hypotonia / diagnosis
Muscle Hypotonia / etiology
Paralysis / diagnosis
Paralysis / etiology