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Overview of included studies for PxMD-PNKD:
Click here for summary of patients' characteristics
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Filter for
all included patients
index patients only
AAO < 50 (adjustable)
AAO >= 50 (adjustable)
females only
males only
homozygous only
heterozygous only
compound heterozygous only
homozygous and compound heterozygous
carrying
definitely pathogenic mutations
probably pathogenic mutations
possibly pathogenic mutations
c.20C>T
c.26C>T
c.97G>C
Country
Belgium
Canada
China
Germany
Greece
Italy
Netherlands
Oman
Poland
Russia
Serbia
Taiwan
Study
Study design
N cases
Ethnicities
Sex
(%
♂
)
Mean AAO (+/- SD)
Reported mutations
Zittel, 2015
Case report/Case series
1
n.a.
0%
0
p.Ala9Val
: het
Ghezzi, 2015
Family study
4
n.a.
50%
5(+/-7)
p.Ala9Val
: het
Liang, 2015
Family study
17
A
100%
0
p.Ala7Val
: het
Fekete, 2013
Case report/Case series
1
n.a.
n.a.
9
p.Ala7Val
: het
Yeh, 2012
Family study
5
A
40%
5(+/-3)
p.Ala7Val
: het
Pons, 2012
Family study
11
C
73%
1(+/-1)
p.Ala7Val
: het
Szczałuba, 2009
Family study
3
C
33%
2
p.Ala9Val
: het
Ghezzi, 2009
Case report/Case series
1
n.a.
100%
n.a.
p.Ala33Pro
: het
Bruno, 2007
Family study
48
n.a.
54%
n.a.
p.Ala7Val
: het
p.Ala9Val
: het
Stefanova, 2006
Family study
5
C
20%
0(+/-0)
p.Ala9Val
: het
Hempelmann, 2006
Family study
6
B
100%
n.a.
p.Ala7Val
: het
Chen, 2005
Family study
14
C
57%
n.a.
p.Ala7Val
: het
p.Ala9Val
: het
Rainier, 2004
Family study
12
C
50%
n.a.
p.Ala7Val
: het
p.Ala9Val
: het
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Dec. 2, 2020. Version: 3.5.95
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