Retinal anomalies in trisomy 18.

Daniel Albert // Publications // Jan 01 1980

PubMed ID: 6903110

Author(s): Fulton AB, Craft JL, Zakov ZN, Howard RO, Albert DM. Retinal anomalies in trisomy 18. Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1980;213(3):195-205. PMID 6903110

Journal: Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. Albrecht Von Graefe’s Archive For Clinical And Experimental Ophthalmology, Volume 213, Issue 3, 1980

The eyes of three patients with trisomy 18, the second most common human autosomal trisomy, were examined histopathologically. In the posterior retina transmission and scanning electron microscopic examinations reveal cytological details characteristic of immature neural retinas. We are able to confirm the report that the posterior retinal pigment epithelium in trisomy 18 has a paucity of mature melanosomes and, in fact, resembles human albino retinal pigment epithelium. The asociation of hypopigmentation and retinal immaturity suggests pigmentation plays a role in the control of the maturation of the neural retina.