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26 March 2024 : Case report  Saudi Arabia

A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant

Challenging differential diagnosis, Management of emergency care, Rare disease, Congenital defects / diseases

Mohammed Shahab Uddin ORCID logo1ACDEF*, AlZahra Y. Alradhi ORCID logo1BFG, Fahad Mushbb N. Alqathani ORCID logo1BFG, Othman Saleh Alessa ORCID logo1BG, Ahmed Nawfal M. Alshammari ORCID logo1BG, Ratna Tripathy2CD, Mohammed Ahmed Alomari1ACDE

DOI: 10.12659/AJCR.942498

Am J Case Rep 2024; 25:e942498

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923