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Galloway syndrome is characterized by the association of nephrotic syndrome and central nervous system anomalies.
Biomarker and diagnostic research for Galloway-Mowat syndrome has been reported in the published literature.
Estimated prevalence: 1-9 in 1,000,000 (Rare).
No clinical trials have been registered for Galloway-Mowat syndrome.
16 publications have been identified in PubMed for Galloway-Mowat syndrome. Research spans Case Report / Case Series (50%), Review / Meta-Analysis (25%), and Basic Science / Preclinical (19%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 8 | 50% |
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 2:11 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Galloway-Mowat syndrome
4 |
25% |
Laboratory research | 3 | 19% |
Testing and diagnosis research | 1 | 6% |
Singh N (2026). [PMID: 42257118](https://pubmed.ncbi.nlm.nih.gov/42257118/). *J Family Med Prim Care*. [Case Report / Case Series]
Li F (2026). [PMID: 41795827](https://pubmed.ncbi.nlm.nih.gov/41795827/). *QJM*. [Diagnostic / Biomarker]
Porowski M (2026). [PMID: 41761595](https://pubmed.ncbi.nlm.nih.gov/41761595/). *Am J Case Rep*. [Case Report / Case Series]
Wei B (2026). [PMID: 41782252](https://pubmed.ncbi.nlm.nih.gov/41782252/). *Ophthalmic Genet*. [Case Report / Case Series]
Kaur N (2026). [PMID: 41689604](https://pubmed.ncbi.nlm.nih.gov/41689604/). *Neurogenetics*. [Case Report / Case Series]
Atallah I (2025). [PMID: 39473271](https://pubmed.ncbi.nlm.nih.gov/39473271/). *Am J Med Genet A*. [Case Report / Case Series]
Yeboah EK (2025). [PMID: 40357071](https://pubmed.ncbi.nlm.nih.gov/40357071/). *Cureus*. [Case Report / Case Series]
Yari A (2025). [PMID: 39661309](https://pubmed.ncbi.nlm.nih.gov/39661309/). *Neurol Sci*. [Case Report / Case Series]
Yang YL (2025). [PMID: 40688758](https://pubmed.ncbi.nlm.nih.gov/40688758/). *Neurol Genet*. [Review / Meta-Analysis]
Eskander J (2025). [PMID: 39572926](https://pubmed.ncbi.nlm.nih.gov/39572926/). *Ophthalmic Genet*. [Review / Meta-Analysis]
AI-curated news mentioning Galloway-Mowat syndrome
Updated Mar 7, 2026
A new study provides a longitudinal genotype-phenotype correlation for OSGEP-associated Galloway-Mowat syndrome, linking prenatal imaging markers to neurologic and renal outcomes throughout the lifespan. This research enhances understanding of the disease's progression and potential early intervention strategies.