| Literature DB >> 28228833 |
Shimpei Baba1, Eri Takeshita1, Hiroko Yamazaki2, Mikako Tarashima3, Masayuki Sasaki1.
Abstract
Joubert syndrome (JS) is a spectrum of genetic disorders characterised by cerebellar and brainstem malformation called "molar tooth sign", resulting in hypotonia, developmental delay, and intellectual disability. Here we describe a young female JS patient with "salt-and-pepper" fundus and inner segment-outer segment junction (IS/OS line) discontinuity, with a lack of external limiting membrane. Ocular coherence tomography (OCT) detected blurred external retinal layers in the macula centre. Although JS patients often have retinal degeneration with varying severity, few investigators have utilised OCT in their investigations. Our findings will help clarify the precise mechanisms of retinal involvement in JS.Entities:
Keywords: Inner segment–outer segment junction disruption; Joubert syndrome; ocular coherence tomography; retinal pigmentation
Year: 2016 PMID: 28228833 PMCID: PMC5278790 DOI: 10.1080/01658107.2016.1236391
Source DB: PubMed Journal: Neuroophthalmology ISSN: 0165-8107