Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings.
Maha A Al-RakanManal D AbothnainMuhammad T AlrifaiMajid AlfadhelPublished in: BMC ophthalmology (2018)
We recommend that clinicians screen patients with GM syndrome for retinal dysfunction and that a skeletal survey should be done to detect developmental dysplasia of the hip (DDH) so as to provide for early intervention.