Comprehensive genetic analysis to identify causative mutations of diseases in the field of pediatric surgery

Comprehensive genetic analysis to identify causative mutations of diseases in the field of pediatric surgery - Comprehensive genetic analysis of diseases in pediatric surgery

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000038902

Enrollment

100

Registered

2020-01-01

Start date

2019-07-22

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Congenital digestive tract atresia, gastrointestinal motility disorder, intestinal malrotation, congenital gastrointestinal malformation, Hirschsprung disease, anorectal malformation, neonatal gastrointestinal perforation, pancreaticobiliary maljunction, biliary atresia, portal hypertension, liver fibrosis, congenital airway disease, pulmonary cystic disease, diaphragmatic hernia, vascular or lymphatic malformation, tumor disease, abdominal wall dysplasia, renal urological malformation, malforma

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Pediatric surgical patients with suspected genetic association

Exclusion criteria

Exclusion criteria: no consent for this study before the operation

Design outcomes

Primary

Measure	Time frame
Identification of causative mutations suggesting possible involvement in the development of each pediatric surgical disease	—

Countries

Japan

Contacts

Public ContactKazuo Oshima

Nagoya University Graduate school of Medicine Department of Pediatric Surgery

oshima_kazuo@hotmail.com052-744-2959

Outcome results