Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2
- Boot, Erik
- Butcher, Nancy J
- Udow, Sean
- Marras, Connie
- Mok, Kin Y
- Kaneko, Satoshi
- Barrett, Matthew J
- Prontera, Paolo
- Berman, Brian D
- Masellis, Mario
- Dufournet, Boris
- Nguyen, Karine
- Charles, Perrine
- Mutez, Eugenie
- Danaila, Teodor
- Jacquette, Aurelia
- Colin, Olivier
- Drapier, Sophie
- Borg, Michel
- Fiksinski, Ania M
- Vergaelen, Elfi
- Swillen, Ann
- Vogels, Annick
- Plate, Annika
- Perandones, Claudia
- Gasser, Thomas
- Clerinx, Kristien
- Bourdain, Frederic
- Mills, Kelly
- Williams, Nigel M
- Wood, Nicholas W
- Booij, Jan
- Lang, Anthony E
- Bassett, Anne S
DOIAbstract
OBJECTIVE: To delineate the natural history, diagnosis, and treatment response of Parkinson disease (PD) in individuals with 22q11.2 deletion syndrome (22q11.2DS), and to determine if these patients differ from those with idiopathic PD. METHODS: In this international observational study, we characterized the clinical and neuroimaging features of 45 individuals with 22q11.2DS and PD (mean follow-up 7.5 ± 4.1 years). RESULTS: 22q11.2DS PD had a typical male excess (32 male, 71.1%), presentation and progression of hallmark motor symptoms, reduced striatal dopamine transporter binding with molecular imaging, and initial positive response to levodopa (93.3%). Mean age at motor symptom onset was relatively young (39.5 ± 8.5 years); 71.4% of cases...
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