Midd
A maternally inherited condition characterized by diabetes and sensorineural deafness with onset after the age of 20, caused by mutation(s) in one of several mitochondrial genes, most frequently the MT-TL1 gene, which encodes the mitochondrial transfer RNA for leucine. Some patients may have additional features observed in mitochondrial disorders, including pigmentary retinopathy, ptosis, cardiomyopathy, myopathy, renal problems, and neuropsychiatric symptoms.
Disease Alternative Name
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AIIMS
Doctor
All India Institute of Medical Science
MBBS
Patwardhan Hospital
B.A.M.S, M.D.
MUHS
M.D Ayurved medicine
Indraprastha Apollo Hospitals, New Delhi
Research Fellow
Government Medical College, Miraj
MBBS
Sai Siddhi Speciality Panchkarma Center Ghatkopar & Govandi
15 Years
Ideal Society of Medical Education and Research Center
MD
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