Labels:text | screenshot | black | black and white | font | document OCR: mia is an Familial hypocalciuric hyper at is frequently autosomal dominant condit unsuccessful found in patients with a hist oidism. The a family history surgery for primary hyperpa characteristics of this conditi xcretion of in siblings or offspring, low r ol/24h) and calcium (<100mg/24h up to 2 magnesium, and usually litt also referred to Patients need to symptomatology. This condi as familial benign hypercalca poor response lial forms of be identified since they have to parathyroidectomy, Unlik ercalcaemia and neonatal period. primary hyperparathyroidism oidism associated hypocalciuria are present fro dent before the In contrast, primary hyperpa with MEN syndromes is rare age of ten.
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