go back

HYPOMAGNESEMIA 6, RENAL; HOMG6

HYPOMAGNESEMIA 6, RENAL; HOMG6
613882
OMIM = Online Mendelian Inheritance of Men
34527
Metal transporter CNNM2
10q24.32
E83.4
rare
autosomal dominant
mutation in the CNNM2 gene
Laboratory findings    Magnesium dec (serum)
Symptoms    headache (severe, recurrent or occipital, migraine)
    muscle weakness
    no clinical symptoms (probably)
    onset, adolescent
    onset, childhood
    onset, infancy
    vertigo, dizziness