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Genetics of megacystis-microlon-intestinal hypoperistalsis syndrome

Genetics of megacystis-microlon-intestinal hypoperistalsis syndrome - Genetics of megacystis-microlon-intestinal hypoperistalsis syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON39441
Enrollment
10
Registered
2011-10-05
Start date
2011-12-01
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

megacystis-microlon-intestinal hypoperistalsis syndrome

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patient: Diagnosis of megacystis-microlon-intestinal hypoperistalsis syndrome Family member: Being a family member of a patient with megacystis-microlon-intestinal hypoperistalsis syndrome

Exclusion criteria

Exclusion criteria: Patient: Not a diagnosis of megacystis-microlon-intestinal hypoperistalsis syndrome Family member: not being a family member of a patient with megacystis-microlon-intestinal hypoperistalsis syndrome

Design outcomes

Primary

MeasureTime frame
Identification of the underlying genes of MMIHS

Secondary

MeasureTime frame
none

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)