Primární hypomagnezemie se sekundární hypokalcemií

Title in English Primary hypomagnesemia with secondary hypocalcemia
Authors

PAPEŽ Jan ŠTARHA Jiří JABANDŽIEV Petr AULICKÁ Štefánia DOLEŽEL Zdeněk

Year of publication 2020
Type Article in Periodical
Magazine / Source Pediatrie pro praxi
MU Faculty or unit

Faculty of Medicine

Citation
Web https://www.pediatriepropraxi.cz/artkey/ped-202002-0010_primarni_hypomagnezemie_se_sekundarni_hypokalcemii.php?back=%2Fsearch.php%3Fquery%3DPrim%25E1rn%25ED%2Bhypomagnezemie%2Bse%2Bsekund%25E1rn%25ED%2Bhypokalcemi%25ED%2Bin%253Aauth%2Bname%2Bkey%2Babstr%
Doi http://dx.doi.org/10.36290/ped.2020.023
Keywords PHSH; hypomagnesemia; hypocalcemia; TRPM6
Description Primary hypomagnesia with secondary hypocalcemia is a rare genetic disorder that appears in early infancy. The cause of this disease is an impaired intestinal absorption of magnesium leading to its low serum level accompanied by hypocalcemia. Typical signs at initial manifestation are generalized seizures, tetany and/or muscle spasms. The prognosis of the disease depends on rapidity and accuracy of the diagnosis.

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