A pre-term baby girl was born following a pregnancy complicated by severe polyhydramnios at a gestational age of 36 weeks. She was initially suffering from respiratory distress consistent with idiopathic respiratory distress syndrome, and altered electrolyte imbalance with hyponatremia, hypokalemia and hypochloremic metabolic alkalosis. However, during the third week of life when she had dehydration along with significant electrolyte imbalance, Bartter\u27s syndrome was considered which was supported by findings of high renin and aldosterone levels. Treatment was done by correction of electrolytes and dehydration along with indomethacin. The drug was well tolerated. The infant showed correction of electrolyte imbalance. The features of this...
Bartter's syndrome is a rare inherited renal tubular disorder. We experienced an 8-month old male pa...
Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivatio...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
A pre-term baby girl was born following a pregnancy complicated by severe polyhydramnios at a gestat...
Ante/neonatal Bartter syndrome (BS) is a rare hereditary disorder. It is characterized by renal salt...
BACKGROUND: Bartter syndrome subtypes are a group of rare renal tubular diseases characterized by im...
Background: Bartter syndrome is a rare autosomal recessive inherited salt wasting tubulopathy, it`s ...
Bartter\u27s syndrome is a rare inherited renal tubular disorder. We experienced an 8-month old male...
Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrom...
Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrom...
Antenatal Bartter syndrome (ABS) is a rare autosomal recessive renal tubular disorder. The defective...
Three and half year old Haleema presented to OPD with complaints of failure to thrive polydipsia and...
Bartter syndrome is an inherited renal tubular disorder associated with hypokalemic alkalosis. The s...
A 2-week-old girl was transferred to our renal ward in February, 2014, from the neonatal intensive c...
Introduction. Pseudo-Bartter syndrome encompasses a heterogenous group of disorders similar to Bart...
Bartter's syndrome is a rare inherited renal tubular disorder. We experienced an 8-month old male pa...
Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivatio...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
A pre-term baby girl was born following a pregnancy complicated by severe polyhydramnios at a gestat...
Ante/neonatal Bartter syndrome (BS) is a rare hereditary disorder. It is characterized by renal salt...
BACKGROUND: Bartter syndrome subtypes are a group of rare renal tubular diseases characterized by im...
Background: Bartter syndrome is a rare autosomal recessive inherited salt wasting tubulopathy, it`s ...
Bartter\u27s syndrome is a rare inherited renal tubular disorder. We experienced an 8-month old male...
Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrom...
Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrom...
Antenatal Bartter syndrome (ABS) is a rare autosomal recessive renal tubular disorder. The defective...
Three and half year old Haleema presented to OPD with complaints of failure to thrive polydipsia and...
Bartter syndrome is an inherited renal tubular disorder associated with hypokalemic alkalosis. The s...
A 2-week-old girl was transferred to our renal ward in February, 2014, from the neonatal intensive c...
Introduction. Pseudo-Bartter syndrome encompasses a heterogenous group of disorders similar to Bart...
Bartter's syndrome is a rare inherited renal tubular disorder. We experienced an 8-month old male pa...
Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivatio...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...