Muscular dystrophy duchenne

An X-linked inherited disorder caused by mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy.

Disease Alternative Name

duchenne muscular dystrophy
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Kanpur
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MBBS

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Ex.central Hospital Dhanbad.1985 ..1993..ex.pathologist .drs Tribedy and Roy Dianostic Lab.kolkata.ex Pathologist.inst of Child Health Kolkata.

Senior Pathologist

School of Tropical Medicine. Kolkata

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Ayurveda Hospital Ganeshwadi Nashik. Maharashtra.

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Grant Medical College

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