what causes Bartter’s Syndrome?
Autosomal recessive
causes severe hypokalaemia due to defective chloride absorption at the NKCC2 in the ascending loop of hence
what are the features of bartters syndrome?
usually presents in childhood eg failure to thrive
polyuria, polydipsia
hypokalaemia
normotension
weakness
which antibodies are present in hashimotos thyroiditis
Anti-thyroid peroxidase antibodies
which antibodies are present in graves disease?
anti- TSH antibodies
what is Gitelman’s syndrome?
Gitelman’s syndrome is a renal tubular disorder characterised by hypokalaemia, metabolic alkalosis, hypocalciuria and hypomagnesaemia.
what causes Gitelaman’s syndrome?
defect in the thiazide-sensitive Na+ Cl- transporter in the distal convoluted tubule.