| Literature DB >> 19022672 |
Mehmet Ruhi Onur1, Utku Senol, Ercan Mihçi, Ersin Lüleci.
Abstract
Lowe (oculocerebrorenal) syndrome is an X-linked recessive disorder characterised by congenital cataract, glaucoma, cognitive developmental delay and renal tubular Fanconi syndrome. In this report we present a patient with Lowe syndrome with a tigroid pattern on cranial MRI, which has not been previously reported as an imaging feature of this syndrome.Entities:
Mesh：
Year: 2008 PMID： 19022672 DOI： 10.1016/j.jocn.2008.02.011
Source DB: PubMed Journal: J Clin Neurosci ISSN： 0967-5868 Impact factor: 1.961