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.
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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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Dr. Nirmal Shah2 Likes5 Answers- Login to View the image
Tibial aplasia and prosthetic Leg restoration. *Chief Complaints* Due to congenital anomalies she walks with abnormal gait patterns. *History* When she was born 28 years ago with such congenital anomalies. Her parents never thought that their 5th girl child would be the same as others 4 . But she had different problems with tibial aplasia and others 4 having complex syndactyly in both hands. Same as their father having complex syndactyly. *Vitals* Unable to perform activities of daily living. *Physical Examination* Problem with walking and gripping and grasping. *Management* 28 years old girl looking for Prosthetics management for tibial aplasia. Our team takes measurements and casting for Prosthetic Leg restoration. Now she walks comfortably with a new prosthetic Leg.
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