{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,7,6]],"date-time":"2024-07-06T07:48:18Z","timestamp":1720252098085},"reference-count":46,"publisher":"Walter de Gruyter GmbH","issue":"11-12","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2015,1,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Although most hypocalcemia with hypomagenesemia in the neonatal period is due to transient neonatal hypoparathyroidism, magnesium channel defects should also be considered.<\/jats:p><jats:p>We report a case of persistent hypomagnesemia in an 8-day-old Hispanic male who presented with generalized seizures. He was initially found to have hypomagnesemia, hypocalcemia, hyperphosphatemia and normal parathyroid hormone. Serum calcium normalized with administration of calcitriol and calcium carbonate. Serum magnesium improved with oral magnesium sulfate. However, 1 week after magnesium was discontinued, serum magnesium declined to 0.5 mg\/dL. Magnesium supplementation was immediately restarted, and periodic seizure activity resolved after serum magnesium concentration was maintained above 0.9 mg\/dL. The child was eventually weaned off oral calcium and calcitriol with persistent normocalemia. However, supraphysiologic oral magnesium doses were necessary to prevent seizures and maintain serum magnesium at the low limit of normal.<\/jats:p><jats:p>As his clinical presentation suggested primary renal magnesium wastage,<\/jats:p><jats:p>Two novel<\/jats:p>","DOI":"10.1515\/jpem-2014-0394","type":"journal-article","created":{"date-parts":[[2015,7,30]],"date-time":"2015-07-30T17:21:27Z","timestamp":1438276887000},"source":"Crossref","is-referenced-by-count":6,"title":["Hypomagnesemia due to two novel TRPM6 mutations"],"prefix":"10.1515","volume":"28","author":[{"given":"Michelle","family":"Coulter","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Caroline","family":"Colvin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bruce","family":"Korf","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ludwine","family":"Messiaen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Benjamin","family":"Tuanama","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael","family":"Crowley","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David K.","family":"Crossman","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kenneth","family":"McCormick","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"374","reference":[{"key":"ref451","article-title":"FR Renal tubular maximimum for magnesium in normal hyperparathyroid and hypoaparthyroid man","volume":"31","author":"Rude","year":"1980","journal-title":"J Clin Endocrinol Metab"},{"key":"ref101","first-page":"385","article-title":"Primary hypomagnesemia with secondary hypocalcemia in an infant","author":"Paunier","year":"1968","journal-title":"Pediatrics"},{"key":"ref371","doi-asserted-by":"crossref","DOI":"10.1093\/hmg\/6.9.1491","article-title":"Familial hypomagnesemia maps to chromosome q not to the chromosome genetic linkage mapping and analysis of a balanced translocation breakpoint","volume":"6","author":"Walder","year":"1997","journal-title":"Hum Mol 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