Galloway Mowat syndrome (GAMOS)
Evidence-based neurology checklist on galloway mowat syndrome (gamos): Genetics The transmission is autosomal recessive Genetic mutations Neurological features Systemic features Magnetic resonance imaging (MRI) features Synonym
Genetics
- The transmission is autosomal recessive
Genetic mutations
Neurological features
Systemic features
Magnetic resonance imaging (MRI) features
Synonym
References
- Yang Y-L, Lee H-F, Chi C-S, Tsai C-R, Liu SN, Wu P-Y. Refining the phenotypic and genotypic spectrum of WDR73-related Galloway-Mowat syndrome. A case series and systematic review. Neurol Genet 2025 (Online ahead of print).
- Delague V, Bareil C, Bouvagnet P, et al. A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze Family. Neurogenetics 2002; 4:23-27.
Related checklists
- Autosomal dominant spastic ataxia (SPAX1)
- Autosomal recessive spastic ataxia 2 (SPAX2)
- Autosomal recessive spastic ataxia 3 (SPAX3)
- Autosomal recessive spastic ataxia 4 (SPAX4)
- Autosomal recessive spastic ataxia 5 (SPAX5)
- Autosomal recessive spastic ataxia 6 (SPAX6)
- Autosomal dominant spastic ataxia 7 (SPAX7)
- Autosomal recessive spastic ataxia 8 (SPAX8)
- PHARC syndrome
- Spastic ataxias: differential diagnosis
