Pediatric Neurology
Volume 33, Issue 3 , Pages 202-205 , September 2005

Neonatal Seizures and Familial Hypomagnesemia With Secondary Hypocalcemia

Received 15 October 2004 ,Accepted 14 March 2005.

References 

  1. Abdulrazzaq YM , Smigura FC , Wettrell G . Primary infantile hypomagnesaemia; report of two cases and review of literature . Eur J Pediatr . 1989;148:459–461
  2. Walder RY , Shalev H , Brennan TM , et al.   Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome (Genetic linkage mapping and analysis of a balanced translocation breakpoint) . Hum Mol Genet . 1997;6:1491–1497
  3. Friedman M , Hatcher G , Watson L . Primary hypomagnesaemia with secondary hypocalcaemia in an infant . Lancet . 1967;1:703–705
  4. Shalev H , Phillip M , Galil A , Carmi R , Landau D . Clinical presentation and outcome in primary familial hypomagnesaemia . Arch Dis Child . 1998;78:127–130
  5. Sutton RA , Domrongkitchaiporn S . Abnormal renal magnesium handling . Miner Electrolyte Metab . 1993;19:232–240
  6. al-Ghamdi SM , Cameron EC , Sutton RA . Magnesium deficiency (Pathophysiologic and clinical overview) . Am J Kidney Dis . 1994;24:737–752
  7. Sutton RA , Dirks H . Disturbances of calcium and magnesium metabolism . In:  Brenner BM ,  Rector FR editor. The kidneys . Vol. 1: Philadelphia: Saunders; 1991;p. 841–887
  8. Quamme GA , Dirks JH . Magnesium metabolism . In:  Narins RG editors. Maxwell and Kleeman’s clinical disorders of fluid and electrolytes metabolism . New York: McGraw-Hill; 1994;p. 373–397
  9. Cole DE , Quamme GA . Inherited disorders of renal magnesium handling . J Am Soc Nephrol . 2000;11:1937–1947
  10. Praga M , Vara J , Gonzalez-Parra E , et al.   Familial hypomagnesemia with hypercalciuria and nephrocalcinosis . Kidney Int . 1995;47:1419–1425
  11. Pronicka E , Gruszczynska B . Familial hypomagnesaemia with secondary hypocalcaemia autosomal or X-linked inheritance? . J Inherit Metab Dis . 1991;14:397–399
  12. Schlingmann KP , Weber S , Peters M , et al.   Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family . Nat Genet . 2002;31:166–170
  13. Milla PJ , Aggett PJ , Wolff OH , Harries JT . Studies in primary hypomagnesaemia (Evidence for defective carrier-mediated small intestinal transport of magnesium) . Gut . 1979;20:1028–1033
  14. Chan GM , Venkataraman P , Tsang RC . The physiology of calcium in the human neonate . In:  Holick MF ,  Gray TK ,  Anast CS editor. Perinatal calcium and phosphorus metabolism . New York: Elsevier; 1983;p. 331–349
  15. Fatemi S , Ryzen E , Flores J , Endres DB , Rude RK . Effect of experimental human magnesium depletion on parathyroid hormone secretion and 1,25-dihydroxyvitamin D metabolism . J Clin Endocrinol Metab . 1991;73:1067–1072
  16. Geven WB , Monnens LA , Willems JL . Magnesium metabolism in childhood . Miner Electrolyte Metab . 1993;19:308–313
  17. Leicher CR , Mezoff AG , Hyams JS . Focal cerebral deficits in severe hypomagnesemia . Pediatr Neurol . 1991;7:380–381
  18. Hall RC , Joffe JR . Hypomagnesemia (Physical and psychiatric symptoms) . JAMA . 1973;224:1749–1751
  19. Chery M , Biancalana V , Philippe C , et al.   Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation (Mapping of the Xp22 chromosome breakpoint) . Hum Genet . 1994;93:587–591
  20. Cockburn F , Brown JK , Belton NR , Forfar JO . Neonatal convulsions associated with primary disturbance of calcium, phosphorus, and magnesium metabolism . Arch Dis Child . 1973;48:99–108

PII: S0887-8994(05)00171-2

doi: 10.1016/j.pediatrneurol.2005.03.009

Pediatric Neurology
Volume 33, Issue 3 , Pages 202-205 , September 2005

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