Retina-Vitreous
2009 , Vol 17 , Num 1
Ophthalmologic Findings in a Case of Sjögren-Larsson Syndrome
1Ondokuz Mayıs Üniversitesi, Tıp Fakültesi, Göz Hast. A.D., Samsun, Uzm. Dr.2Ondokuz Mayıs Üniversitesi, Tıp Fakültesi, Göz Hast. A.D., Samsun, Yard. Doç. Dr.
3Ondokuz Mayıs Üniversitesi, Tıp Fakültesi, Göz Hast. A.D., Samsun, Prof. Dr. Sjögren-Larsson syndrome (SLS) is a recessively inherited disorder characterized by congenital icthyosis, spastic diplegia and mental retardation. The disorder is caused by mutations in the aldehyde dehydrogenase family 3, subfamily A2 gene on 17th cromosome. Patients exibit highly charecteristic bilateral, glistening yellow-white retinal dots from the age of 1 to 2 years onward. We report on ophthalmological features of SLS in our 9 years old female patient. Keywords : Sjögren-Larsson syndrome, crystalline retinopathy, ichthyosis, mental retardation