Moreover, the onset in most cases is several months or even years after the inciting delivery, so it is often misrecognized selleckchem and not adequately treated. Hyponatremi and hypoglicemi that have been rarely reported in the literature. Case Report: A 47-year-old woman, a housewife, was admitted because disturbed consciousness. She had a history of postpartum hemorrhage which had occurred 15 years previous. Amenorrhea and failure to lactate developed thereafter. Fatigue and dry skin were also found. Physical examination revealed a chronically ill looking. She was drowsy, her fluid status was euvolemic, and her conjunctiva appeared anemic. Laboratory data were as follows:

hemoglobin 7, 8 g/dl, the random blood glucose 40 g/dl and the serum sodium 108 meq/L with low serum osmolality and elevated urine sodium. Moreover, the investigations also showed a low of FSH, LH and prolactin. Magnetic Resonance Imaging

of the brain showed an “empty sella” appearance. Thus, a diagnosis of Sheehan MEK inhibitor syndrome was made. Hyponatremia and hypoglycemia that was improved after replacement with glucocorticoids. Conclusions: This case illustrates that Sheehan’s syndrome whose first presentation was with hyponatraemia and hypoglycaemia that have been rarely reported in the literature. Early diagnosis and appropriate treatment are necessary to reduce the morbidity and mortality of patients. Key words: Sheehan Syndrome, Hyponatremia and Hypoglycemia, Empty sella. 283 MILD PERSISTENT HYPERKALEMIA: AN IMPORTANT DIAGNOSTIC CLUE IN SHORT STATURE S CAMPBELL, A WALKER, J KAUSMAN, C QUINLAN Royal Children’s Hospital – Nephrology Department, Melbourne, Australia Aim: The case is of a 10-year-old female who presented

as a diagnostic dilemma to multiple paediatric physicians with key features short stature & hyperkalemia. Background: She initially presented with Perthes disease of both hips was then noted to have a height on the 3rd centile, with mid-parental height expectation of a 10th centile. She was found to be normotensive (50th centile), and without dysmorphic features. Investigations revealed a persistent hyperkalemia (average = 6.2 (3.5–5.5 mmol/L)), in the presence of low/normal aldosterone level (55U/L), and low renin ≤0.2 (1.0–4.0). Sitaxentan Plasma creatinine was normal (36 mmol/L) as was urinary potassium excretion (91 mmol/L). A venous gas demonstrated a mild metabolic acidosis (pH 7.32, BE = −4). Methods: A diagnostic trial of hydrochlorothiazide was successful in resolving her hyperkalemia. Results: The clinical & biochemical picture is consistent with that of Type II pseudohypoaldosteronism (PHAII), specifically Spitzer-Weinstein syndrome. Conclusions: A rare disorder, inherited in an autosomal dominant manner involving the WNK1 and WNK4 genes. WNK kinases are named so due to a lack of lysine in the ATP binding cassette of the catalytic region.