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Coexistence of hereditary spherocytosis and Gilbert syndrome with SLC4A1 gene mutation: case report and literature review

Coexistence of hereditary spherocytosis and Gilbert syndrome with SLC4A1 gene mutation: case report and literature review

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104307
Enrollment
Unknown
Registered
2025-06-15
Start date
2023-02-15
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Hereditary spherocytosis

Interventions

Observation group:None

Sponsors

Northern Jiangsu People’s Hospital of Jiangsu Province
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: One patient was discharged on April 8, 2021 with clinically confirmed HS and GS

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
SLC4A1 gene;UGT1A1 gene;—

Countries

China

Contacts

Public ContactFangfang Wang

Northern Jiangsu People’s Hospital of Jiangsu Province

d160118@yzu.edu.cn+86 180 5106 0607

Outcome results

None listed

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