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McCune-Albright syndrome Clinical Registry of China

McCune-Albright syndrome Clinical Registry of China

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300076039
Enrollment
Unknown
Registered
2023-09-22
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-09-26

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

Conditions

McCune-Albright syndrome

Interventions

Sponsors

the First Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Patients with typical clinical manifestations suspected of MAS (=1 of the three major diseases of Cafe-au-lait, precocious puberty (hyperfunction of endocrine glands ), and bone fibrous dysplasia) and pathogenic variation of the GNAS gene. 2. Patients diagnosed MAS with the three typical main symptoms but the GNAS1 gene mutations were not detected.

Exclusion criteria

Exclusion criteria: 1, Patients have less than three typical main symptoms ( Cafe-au-lait, precocious puberty(hyperfunction of endocrine glands), and bone fibrous dysplasia) and the GNAS1 gene mutations were not detected. 2. Patients with MAS were reluctant to join the cohort of researchers.

Design outcomes

Primary

MeasureTime frame
cafe-au-late spots;hyperfunction of endocrine glands;bone fibrous dysplasia;

Countries

China

Contacts

Public ContactWang Chunlin

the First Affiliated Hospital, Zhejiang University School of Medicine

hzwangcl@zju.edu.cn+86 571 8723 3319

Outcome results

None listed

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