Rare genetic disorders include Ehlers-Danlos syndrome, mitochondrial disease, and Fraser syndrome. But what is Fraser syndrome? How common is Fraser syndrome? What is the Fraser syndrome life ...

Figure 1: Grip1 mutants phenocopy mice lacking the Fraser syndrome protein Fras1. Consistent with the protein-protein interaction described above and the overlapping expression patterns in vivo ...

Figure 1: Mapping the my Ucl locus to mouse chromosome 3 (MMU3). The proband was born at 32 weeks of gestation to parents who were first cousins, once removed; weighed 1.34 kg; and died within 1 h ...

Fraser syndrome is a poorly understood disorder that can affect multiple parts of the body, but the majority of cases involve the eyes. Canadian geneticist C.R. Fraser described the disease in 1962.

Back to Healio A systematic periocular surgical approach proved effective in managing structural abnormalities associated with Fraser syndrome, according to a study. "Although Fraser syndrome is ...

This defect is linked to Fraser syndrome deafness in humans. Reporting in the Aug. 1 issue of the journal Development, they identify a potential developmental pathway worthy of more scrutiny in ...

Christmas is Aadam's favourite time of year, but with a visual impairment through Fraser Syndrome, he can sometimes be left out of celebrations if they aren't accessible. Now the Royal National ...

Christmas is Aadam's favourite time of year, but with a visual impairment through Fraser Syndrome, he can sometimes be left out of celebrations if they aren't accessible. Now the Royal National ...

Reporting in the Aug. 1 issue of the journal Development, they identify a potential developmental pathway worthy of more scrutiny in future research into Fraser syndrome, a many-faceted and rare ...