ALMS1 and Nystagmus: A pathogenic mutation in the ALMS1 gene (c.8441C>A, p. S2814*) has been discovered in another whole-exome sequencing study conducted on a 5-year-old Saudi girl who was born into a consanguineous marriage and had photophobia, noticeable nystagmus, and retinal abnormalities with short fingers tapering [16].