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A case report of a baby with Cushing syndrome carrying a PRKAR1A gene mutation

A case report of a baby with Cushing syndrome carrying a PRKAR1A gene mutation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102156
Enrollment
Unknown
Registered
2025-05-09
Start date
2022-10-21
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Cushing syndrome

Interventions

Study case:None

Sponsors

Fujian Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Single case report, no inclusion criteria.

Exclusion criteria

Exclusion criteria: None.

Design outcomes

Primary

MeasureTime frame
Whole-exome genome;—

Secondary

MeasureTime frame
Sex hormone levels;—

Countries

China

Contacts

Public ContactGao Jiaying

Fujian Children's Hospital

gphoebe@163.com+86 183 2196 2429

Outcome results

None listed

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