Searching for the genetic cause of Galloway-Mowat Syndrome

Identification of causative genes in Galloway-Mowat Syndrome - Galloway-Mowat Syndrome gene study

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000058802

Enrollment

Registered

2025-08-15

Start date

2025-06-04

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

Galloway-Mowat Syndrome

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients whom attending physician has diagnosed as having Galloway-Mowat syndrome or suspected Galloway-Mowat syndrome, in accordance with the following diagnostic criteria of Japan Intractable Disease Information Center.

Exclusion criteria

Exclusion criteria: Patients who did not provide informed consent to participate in the study.

Design outcomes

Primary

Measure	Time frame
To analyze genotype-phenotype correlations -i.e., associations between genetic variants and clinical manifestations- in patients in Japan with confirmed or suspected Galloway-Mowat Syndrome and, where conset is obtained, their biological relatives.	—

Countries

Japan

Contacts

Public ContactChikako Terano

Kitasato University School of Medicine Department of Pediatrics

chikatrex@yahoo.co.jp042-778-8111

Outcome results