A multicenter study of genotypes and clinical phenotypes and cognitive function interventions in Williams syndrome

multicenter study of genotypes and clinical phenotypes and cognitive function interventions in Williams syndrome

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000040189

Enrollment

Unknown

Registered

2020-11-24

Start date

2021-01-01

Completion date

Unknown

Last updated

2021-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Williams syndrome

Interventions

group 1:non

group 2:cognitive intervention

Eligibility

Sex/Gender

Male

Age

1 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Aged 1-18 years; 2. The WS clinical score of the American academy of pediatrics > 3 or confirmed by MLPA, CMA.

Exclusion criteria

Exclusion criteria: non

Design outcomes

Primary

Measure	Time frame
clinical phenotype;Gene test;	—

Countries

China

Contacts

Public ContactXuekun Li

Children's Hospital Zhejiang University School of Medicine

158965672@qq.com+86 13857162542

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026