Status epilepticus as the only presentation of the neonatal Bartter syndrome

Bartter syndrome is a rare hereditary (autosomal recessive) salt-losing tubulopathy characterized by hypokalemia, hypochloremia, metabolic alkalosis, and normal blood pressure with hyperreninemia, The underlying renal abnormality results in excessive urinary losses of sodium, chloride, and potassium...

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Bibliographic Details
Main Authors: Soumya Patra, Mithun C Konar, Rajarshi Basu, Ajoy K Khaowas, Soumyadeep Dutta, Debanjali Sarkar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-01-01
Series:Indian Journal of Endocrinology and Metabolism
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Online Access:http://www.ijem.in/article.asp?issn=2230-8210;year=2012;volume=16;issue=2;spage=300;epage=302;aulast=Patra
Description
Summary:Bartter syndrome is a rare hereditary (autosomal recessive) salt-losing tubulopathy characterized by hypokalemia, hypochloremia, metabolic alkalosis, and normal blood pressure with hyperreninemia, The underlying renal abnormality results in excessive urinary losses of sodium, chloride, and potassium. We report a case of a four-month-old infant with neonatal Bartter syndrome, who presented only with status epilepticus. To the best of our present knowledge, there is no reported case of Bartter syndrome who presented with status epilepticus.
ISSN:2230-8210
2230-9500