منابع مشابه
Woman with hypomagnesemia and hypocalcemia.
A 71-year-old woman was referred to the endocrinology clinic after several years of unresolved hypomagnesemia that required numerous hospital admissions to receive intravenous magnesium. She previously presented with palpitations on 3 occasions, and once with diarrhea and vomiting. The blood tests on all 4 presentations demonstrated severe hypomagnesemia (Table 1). Her medical history included ...
متن کاملHypomagnesemia predicts postoperative biochemical hypocalcemia after thyroidectomy
BACKGROUND To investigate the role of magnesium in biochemical and symptomatic hypocalcemia, a retrospective study was conducted. METHODS Less-than-total thyroidectomy patients were excluded from the final analysis. Identified the risk factors of biochemical and symptomatic hypocalcemia, and investigated the correlation by logistic regression and correlation test respectively. RESULTS A tot...
متن کاملFamilial Hypomagnesemia with Secondary Hypocalcemia Mimicking Neurodegenerative Disorder.
BACKGROUND Familial hypomagnesemia with secondary hypocalcemia is a genetic disorder of magnesium metabolism that presents with refractory seizures in infancy. CASE CHARACTERISTICS We herein report an infant with familial hypomagnesemia who presented as medically-refractory seizures and had cerebral atrophy on neuroimaging. Interestingly he had lost previous two siblings because of lack of co...
متن کاملPrimary hypomagnesemia with secondary hypocalcemia in an infant.
A 2-month old girl was transferred from General Hos pital Kurunegala to the Lady Ridgeway Hospital (LRH) in September 1998 with a history of uncontrolled generalised fits from the age of 6 weeks. Before 6 weeks the baby-had been apparently normal. She is a product of a first cousin marriage. The other two children are in good health. The birth and neonatal histories were normal. The birth weig...
متن کاملNovel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia.
Primary hypomagnesemia with secondary hypocalcemia is a rare autosomal recessive disorder characterized by profound hypomagnesemia associated with hypocalcemia. Pathophysiology is related to impaired intestinal absorption of magnesium accompanied by renal magnesium wasting as a result of a reabsorption defect in the distal convoluted tubule. Recently, mutations in the TRPM6 gene coding for TRPM...
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ژورنال
عنوان ژورنال: Clinical Chemistry
سال: 2015
ISSN: 0009-9147,1530-8561
DOI: 10.1373/clinchem.2014.229005