Autosomal dominant primary hypomagnesemia with hypocalciuria

Disease Export to PDF
Name:
Autosomal dominant primary hypomagnesemia with hypocalciuria
Description:
A mild form of familial primary hypomagnesemia (FPH), characterized by extreme weakness, tetany and convulsions. Secondary disturbances in calcium excretion are observed.
ORPHAcode:
34528
Synonyms:
HOMG2
Isolated autosomal dominant hypomagnesemia
Isolated renal magnesium wasting
Renal hypomagnesemia type 2
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14