Skip to content
Research Article Open access CC BY 4.0

Familial Hypomagnesemia with Secondary Hypocalcemia: A Challenging Medical Affair

S. Aithmadouch, A.laaraj, A. Radi, R. Abikassem

Asian Journal of Advanced Research and Reports · pp. 412–416 · Published 18 Dec 2024

10.9734/ajarr/2024/v18i12838

Abstract

Familial or genetic hypomagnesemia with secondary hypocalcemia is a disease typically presenting with epilepsy and characterized by low blood levels of magnesium and calcium and metabolic bone disease, and is caused by mutations in the TRPM6 genes. Various factors such as low dietary intake and poor absorption of magnesium in the gut, affect magnesium balance. Hypomagnesemia with secondary hypocalcemia is rare, and therefore there are no large epidemiological studies reflecting the global distribution of these conditions. We report in this article a case of a female infant with a diagnosis of congenital hypomagnesemia with secondary hypocalcemia. In daily clinical practice, one can usually see it in connection with neonates. According to the literature, mutations of TRPM6 account for about 40–50% of hypomagnesemia patients with secondary hypocalcemia.

Hypomagnesemia hypocalcemia TRPM6 mutation seizure

Cited by 0

No indexed citations yet.

Article metrics

Real usage data collected on this platform.

0

Page views

0

PDF downloads

0

Outbound clicks

0

Citations

Views by country

Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".

No views recorded yet.

Traffic sources

Referring site, by host.

No traffic recorded yet.

Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.