PRESENTATION OF CASE A 22 years old G2 P1 D1 came with complaints of shivering of both upper limb and lower limb. She was diagnosed with Gitelman syndrome in previous pregnancy. Previous was a preterm delivery due to polyhydramnios and the baby died at 12 days of life due to some congenital malformation of heart. In previous pregnancy, patient presented with paralysis at 6 months of gestation and was treated conservatively by correcting the electrolytes level. In the present pregnancy, patient had persistent hypokalaemia and hypomagnesaemia, which was treated. Anomaly scan was done. No gross anomaly was detected. Patient is symptomatically better and she is continuing her pregnancy, hope better outcome since GS has no adverse e...
We report the case of a 43-year-old woman with sero-positive nodular erosive rheumatoid arthritis wh...
Gitelman syndrome is a rare, autosomal recessive, renal tubular salt wasting disorder characterized ...
An 18-year-old woman with Gitelman syndrome (GS) associated with idiopathic intracranial hypertensio...
Gitelman's syndrome (GS), a rare renal disorder, results in hypokalaemia, hypomagnesaemia, hypo...
Gitelman syndrome (GS) is an autosomal-recessive condition characterized by hypokalemia, hy-pomagnes...
Gitelman's syndrome (GS), a rare renal disorder, results in hypokalaemia, hypomagnesaemia, hypo...
Gitelman syndrome is a rare renal tubule disease characterized by hypokalaemia, metabolic alkalosis,...
It is widely assumed that Gitelman syndrome is a rare genetic disorder with such electrolyte imbalan...
Introduction. Gitelman’s syndrome (GS) is an autosomal recessive inherited defect in the thiazide-se...
Gitelman syndrome is a rare renal tubule disease characterized by hypokalaemia, metabolic alkalosis,...
Gitelman syndrome (GS) is a rare renal disorder, and little is known about its impact on pregnancy. ...
Abstract Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is charact...
Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is characterized by...
Gitelman syndrome is one of the few inherited causes of metabolic alkalosis due to salt losing tubul...
Gitelman's syndrome is primarily renal tubular hypokalemic metabolic alkalosis with hypocalciuria a...
We report the case of a 43-year-old woman with sero-positive nodular erosive rheumatoid arthritis wh...
Gitelman syndrome is a rare, autosomal recessive, renal tubular salt wasting disorder characterized ...
An 18-year-old woman with Gitelman syndrome (GS) associated with idiopathic intracranial hypertensio...
Gitelman's syndrome (GS), a rare renal disorder, results in hypokalaemia, hypomagnesaemia, hypo...
Gitelman syndrome (GS) is an autosomal-recessive condition characterized by hypokalemia, hy-pomagnes...
Gitelman's syndrome (GS), a rare renal disorder, results in hypokalaemia, hypomagnesaemia, hypo...
Gitelman syndrome is a rare renal tubule disease characterized by hypokalaemia, metabolic alkalosis,...
It is widely assumed that Gitelman syndrome is a rare genetic disorder with such electrolyte imbalan...
Introduction. Gitelman’s syndrome (GS) is an autosomal recessive inherited defect in the thiazide-se...
Gitelman syndrome is a rare renal tubule disease characterized by hypokalaemia, metabolic alkalosis,...
Gitelman syndrome (GS) is a rare renal disorder, and little is known about its impact on pregnancy. ...
Abstract Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is charact...
Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is characterized by...
Gitelman syndrome is one of the few inherited causes of metabolic alkalosis due to salt losing tubul...
Gitelman's syndrome is primarily renal tubular hypokalemic metabolic alkalosis with hypocalciuria a...
We report the case of a 43-year-old woman with sero-positive nodular erosive rheumatoid arthritis wh...
Gitelman syndrome is a rare, autosomal recessive, renal tubular salt wasting disorder characterized ...
An 18-year-old woman with Gitelman syndrome (GS) associated with idiopathic intracranial hypertensio...