RT Journal Article SR Electronic T1 HaNDL with bilateral central venous occlusions JF BMJ Neurology Open JO BMJ Neurol Open FD BMJ Publishing Group Ltd SP e000043 DO 10.1136/bmjno-2020-000043 VO 2 IS 1 A1 Wendy Wang A1 Heather G Mack A1 Richard Stawell A1 Owen White A1 John Waterston YR 2020 UL http://neurologyopen.bmj.com/content/2/1/e000043.abstract AB Background The syndrome of Headache and focal Neurological Deficits with cerebrospinal fluid Lymphocytosis (HaNDL) is considered a rare, idiopathic and self-limited condition.Methods We present a patient with HaNDL who had unique findings of florid optic disc haemorrhages from bilateral central retinal vein occlusions.Results Our patient made a full recovery with conservative management.Conclusion It is important for medical attendants to recognise that HaNDL syndrome can be associated with neuro-ophthalmic complications.