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Clinical study of DGAT1 gene defect

Clinical study of DGAT1 gene defect

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048204
Enrollment
Unknown
Registered
2021-07-04
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-03-14

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

Conditions

DGAT1 gene defect

Interventions

case series:None

Sponsors

Seventh Medical Center of Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 17 Years

Inclusion criteria

Inclusion criteria: The gene mutation of diacylglycerol Acyltransferase-1 was detected. Most of the newborns had diarrhea, manifested as chronic diarrhea, vomiting and poor growth and development. The prognosis can be improved by adjusting diet and intravenous nutrition.

Exclusion criteria

Exclusion criteria: Duodenal mucosal microscopic examination showed microvillous inclusion disease and congenital tufted enteropathy.

Design outcomes

Primary

MeasureTime frame
Intervention effect;Diagnostic accuracy;Prognosis;—

Countries

China

Contacts

Public ContactXu Xuan

Seventh Medical Center of Chinese PLA General Hospital

xuxuan2008-gz@163.com+86 15810286321

Outcome results

None listed

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