Neonatal Bartter’s syndrome is a rare autosomal recessive congenital renal tubular disorder that characterized by severe polyhydramnios resulting from intrauterine onset polyuria. It is a life-threatening condition because of its severe clinic course. We report here two rare cases of neonatal Bartter’s syndrome in order to stress that early indomethacin treatment in addition to appropriate fluid and electrolyte support would be an appropriate approach
Neonatal Bartter's syndrome is a rare autosomal recessive congenital renal tubular disorder that characterized by levels of polyhydramnios resulting from intrauterine onset polyuria. It is a life-threatening condition because of its level clinic course. We report here two rare cases of neonatal Bartter's syndrome in order to stress that early indomethacin treatment in addition to appropriate fluid and electrolyte support would be an appropriate approach
Alan : Sağlık Bilimleri
Dergi Türü : Uluslararası
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