From: Long-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3mutation; case report and review of the literature
Individual1
Ref. range
Unit
I-2
II-2
II-3
II-4
II-5
III-1
III-3
Genotype2
M/m
m/m
M/M
i-FGF23
21.6-70.23
pg/ml
66.3
51
26.8
33.0
12
47.2
53
c-FGF23
10-802
RU/ml
32.2
25.2
120
34.8
210
17.2
20.2