Page 93 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma

Parkinsonism in GNDs
sTable 3. continued
Search
date and
study
number
First author Year of
publication Journal Reason for exclusion
29 Carecchio 2017 Eur J Neurol Other: Information
on the whole group
is provided, including
genetic disorders not
meeting our definition.
30 Carecchio 2011 movement disord No clear genetic
diagnosis
31 Castello 2012 clin neuropathol parkinsonism unclear
32 Chitty 2016 aust nz j psychiat No clear genetic
diagnosis
33 Cubells 2010 Neuropsychopharmacol not relevant
34 Cukiert 2009 epilepsia No clear genetic
diagnosis
35 de Kuijper 2013 res dev disabil No clear genetic
diagnosis
36 De Lonlay 2000 j inherit metab dis parkinsonism unclear
37 Demirbas 2018 mol genet metab parkinsonism unclear
38 Deuel 2019 Neurology parkinsonism unclear
39 Dhivya 2016 Int J Hum Genet Other: Aim, methods,
and results all unclear
40 Dobyns 1993 Neurology No clear genetic
diagnosis
41 Dufournet 2015 Eur J Neurol no new data
42 Dulovic 2016 movement disord parkinsonism unclear
43 Ekinci 2004 movement disord No clear genetic
diagnosis
44 Elahi 2017 movement disord no new data
45 Fan 2020 movement disord parkinsonism unclear
46 Fanella 2019 J Med Genet parkinsonism unclear
47 Finsterer 2011 acta neurol belg Other: heterozygous for
autosomal recessive
disorder; usually
asymptomatic
48 Fitzgerald 1990 neurology no new data
49 Fraser 2019 Ann Neurol No clear genetic
diagnosis
50 Galati 2015 j neuropsych clin n No clear genetic
diagnosis
51 Gao 2020 movement disord no new data
52 Gascon 1994 brain & development parkinsonism unclear
53 Grant 1992 eur j pediatr No clear genetic
diagnosis
54 Gunzler 2007 movement disord No clear genetic
diagnosis
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