Ante/neonatal Bartter syndrome (BS) is a rare hereditary disorder. It is characterized by renal salt wasting, hypokalaemic metabolic alkalosis, high renin and aldosterone but normal blood pressure. We report a low birth weight newborn baby who presented with repeated apnoea shortly after birth as well as hyponatraemia, hypochloraemia, hyperkalaemia and metabolic acidosis. Her biochemical features mimicked pseudohypoaldosteronism but with initial hypertension, which had not been described in BS. Her subsequent genetic study confirmed two novel heterozygous mutations in the Exon 5 of KCNJ1 compatible with Type II BS
Mutations in the ROMK1 potassium channel gene (KCNJ1) cause antenatal/neonatal Bartter syndrome type...
Bartter syndrome is a rare hereditary (autosomal recessive) salt-losing tubulopathy characterized by...
Bartter syndrome is a rare inherited salt-losing renal tubular disorder characterized by secondary h...
Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivatio...
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 syndrome (BS) is an autosomal recessively inherited rare renal tubular disorder characterize...
A pre-term baby girl was born following a pregnancy complicated by severe polyhydramnios at a gestat...
Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrom...
Variants of inherited hypokalemic tubulopathies follow autosomal recessive inheritance and share cha...
Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrom...
Background. Ante/neonatal Bartter syndrome (BS) is a hereditary salt-losing tubulopathy due to mutat...
Bartter syndrome comprises a group of rare autosomal-recessive salt-losing disorders with distinct p...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
Item does not contain fulltextBartter syndrome encompasses a variety of inheritable renal tubular tr...
Mutations in the ROMK1 potassium channel gene (KCNJ1) cause antenatal/neonatal Bartter syndrome type...
Bartter syndrome is a rare hereditary (autosomal recessive) salt-losing tubulopathy characterized by...
Bartter syndrome is a rare inherited salt-losing renal tubular disorder characterized by secondary h...
Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivatio...
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 syndrome (BS) is an autosomal recessively inherited rare renal tubular disorder characterize...
A pre-term baby girl was born following a pregnancy complicated by severe polyhydramnios at a gestat...
Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrom...
Variants of inherited hypokalemic tubulopathies follow autosomal recessive inheritance and share cha...
Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrom...
Background. Ante/neonatal Bartter syndrome (BS) is a hereditary salt-losing tubulopathy due to mutat...
Bartter syndrome comprises a group of rare autosomal-recessive salt-losing disorders with distinct p...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
Item does not contain fulltextBartter syndrome encompasses a variety of inheritable renal tubular tr...
Mutations in the ROMK1 potassium channel gene (KCNJ1) cause antenatal/neonatal Bartter syndrome type...
Bartter syndrome is a rare hereditary (autosomal recessive) salt-losing tubulopathy characterized by...
Bartter syndrome is a rare inherited salt-losing renal tubular disorder characterized by secondary h...