Non-drug Study to Evaluate the Suitability of Neurocognitive Tests and Functioning Scales for the Measurement of Cognitive and Functioning Changes in Children With Down Syndrome

Inclusion Criteria:

- Males and females aged 6 to 11 with diagnosis of Down syndrome (Trisomy 21). Children
may have standard trisomy 21, Robertsonian translocation, isochromosome 21 (so called
21q21q Robertsonian translocation), Down syndrome with reciprocal translocation or
mosaicism.

- Down syndrome children meeting clinical diagnostic criteria for generalized anxiety
disorders, autism spectrum disorder, attention deficit and hyperactivity disorder, can
participate in the study provided they are considered clinically stable or on stable
medication for at least 8 weeks prior to the baseline visit.

- Parent or legal guardian/representative and caregiver willing to give written informed
consent.

- Subjects with sufficient vision and hearing to engage in study evaluations as referred
by their parents. Mild hearing loss will be allowed.

Exclusion Criteria:

- Children who may not be able to comply with the protocol or perform the outcome
measures due to significant hearing or visual impairment or other issues judged
relevant by the investigators

- Significant sleep disruption or moderate to severe untreated obstructive sleep apnea.

- Any condition which would make the individual or the caregiver, in the opinion of the
investigator, unsuitable for the study.