hrp0094p1-17 | Bone A | ESPE2021
, Anjum Muhammad Nadeem
, Saeed Anjum
, Shaheen Tahir
, Cheema Huma Arshad
Background: Hypomagnesemia type 1 (HOMG1) is a rare autosomal recessive condition due to TRPM6 mutation, leading to decrease intestinal magnesium absorption.Objective: To determine the clinical spectrum of HOMG1 due to TRPM6 mutation at a tertiary centre.Case Series: Seven patients (all male) from six different families of hypomagnesemia type 1 due to homozygous TRPM6 mut...