Duchenne muscular dystrophy
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.
Recent Cases of Duchenne muscular dystrophy
Browse recently discussed Duchenne muscular dystrophy cases by specialists202 Views
, 2 Likes
, 10 Answers
Top Cases of Duchenne muscular dystrophy
Selected by editors, top cases are known for unique problem or best solution116 Views
, 3 Likes
, 13 Answers
Top Duchenne muscular dystrophy Doctors on Curofy
Top doctors who continously share their opinions on Duchenne muscular dystrophyNational Institute of Medical Science
Md Paediatrics
National Institute of Medical Science
MD pediatrics
Medical Component OfHCM
Remained Incharge Medical Officer with Hon'Ble C.M of J and K for More Than 20 Years from Jan 2000 To October 2020
Govt. Medical College, Jammu
M.S (General Surgery )
Ross Clinics , Sector 23
Consultant Physiotherapist
Swatantra Institute Of Physiotherapy And Rehabilitation
B.P.T
Self Emploid(private Clinic)
Morbi
Shri M P Shah Medical College Jamnagar
M B B S
GRH Madurai
Mbbs
Madurai Medical College
MBBS
Trending Diseases
Trending Cases
- Login to View the image
50 year female having cervical spondylitis symptoms (radiating to hands, neck stiffness, ) from past 15 years.
Wahib Zaidi0 Like5 Answers - Login to View the image
M.43yrs Pain and stiffness Neck and back 2years
Dr. Syam Sundar Patro1 Like4 Answers - Login to View the image
Quick Brains Quiz - 3rd November 2024 Topic - Irritable Bowel Syndrome Check how quickly can you solve these questions using your clinical knowledge.
Curofy Quiz0 Like0 Answer - Login to View the image
Check out the answers of Quick Brains Quiz posted on - 3rd November 2024 Topic - Irritable Bowel Syndrome.
Curofy Quiz0 Like0 Answer
50 Views
, 1 Like
, 1 Answer