Table 2 Results of glucose excretion studies and mutation analysis in patients with familial renal glucosuria and their family members.

From: A recurrent deletion in the SLC5A2 gene including the intron 7 branch site responsible for familial renal glucosuria

Family-member

24 h Glucose excretion (g/24 h/1.73 m2)

Allele 1

Allele 2

Ic (proband)

10.56

p.S335G

p.Q448R+ p.G580D

Ia (father)

0.15

p.S335G

WT

Ib (mother)

0.10

WT

p.Q448R+ p.G580D

IIc (index case)

1.96

c.886(-10_-31)del

WT

IIa (father)

1.88

c.886(-10_-31)del

WT

IIb (mother)

0.08

WT

WT

IIIc (proband)

1.77

c.886(-10_-31)del

WT

IIIa (father)

2.04

c.886(-10_-31)del

WT

IIIb (mother)

2.3a

WT

WT

IIId (brother)

0.01

WT

WT

IIIe (daughter)

0.02

WT

WT

IVc (proband)

1.66

c.886(-10_-31)del

WT

IVa (father)

Φ

WT

WT

IVb (mother)

Φ

c.886(-10_-31)del

WT

Vc (proband)

12.74

c.886(-10_-31)del

WT

Va (father)

0.03

WT

WT

Vb (mother)

0.88

c.886(-10_-31)del

WT

Via (proband)

1.34

p.A474P

WT

VIb (son)

2.25

p.A474P

WT

VIIc (proband)

50.68

c.886(-10_-31)del

c.886(-10_-31)del

VIIa (father)

1.44

c.886(-10_-31)del

WT

VIIb (mother)

2.45

WT

c.886(-10_-31)del

VIId (daughter)

1.78

c.886(-10_-31)del

WT

VIIIa (proband)

1.58

p.K131N

WT

VIIIb (spouse)

0.17

WT

WT

VIIIc (son)

1.37

p.K131N

WT

  1. Patients with familial renal glucosuria are indicated by boldface; wt, wild type; Ø, no glucosuria by dipstick method;
  2. aat elevated blood glucose concentrations as a result of type 2 diabetes.