Year-end Sale % OFF 
Abstract
MIDD (Maternally Inherited Diabetes and Deafness) and MELAS (Mitochondrial Encephalomyopathy with Lactic Acidosis and Stroke-like episodes) are related syndromes both associated with the m.3243A>G mutation. A patient with this mutation, previously diagnosed with MIDD, is described who showed two remarkable clinical features: severe insulin resistance and the development of MELAS over time.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
