Late-onset mitochondrial encephalomyopathy with lactic acid and stroke-like episodes (MELAS), defining symptomology

With interest we read Finsterer et al.'s response [1] to our manuscript ‘Case Report: 5 Year Follow-Up of Adult Late-OnsetMitochondrial Encephalomyopathy with Lactic Acid and Stroke-Like Episodes (MELAS)’ [2]. We have the following responses: Regarding the lack of theMRIfigure, theMRIwas performed at an outside hospital. As a result an MRI figure was not available despite efforts to the contrary and only clinical interpretationswere available. Upon review of theMRI report, it was determined that the patient showed a non-vascular distribution. While it remains possible the patient suffered an ischemic stroke, there is always an element of presumption in imaging-making ischemic stroke a possibility. In response to the question of whether our patient's MELAS was indeed ‘late-onset’ we disagree that the treating physicians should have considered MELAS in the patient's 30s due to short stature, hypothyroidism andmild migraines, the latter of which did not require medical intervention. Whilst there may indeed be a link or associated between these symptoms and MELAS, when compared with classical MELAS cases, our patient's onset of major neurological symptoms was clearly much later. Given that short stature, hypothyroidism and hypoacusis are not enough to diagnose a patient with MELAS by defined diagnostic criteria, we find it hard to expect a physician to make a diagnosis of MELAS on these symptoms, unless they are an expert in mitochondrial