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Homeopathy World Community

Creating Waves of Awareness

Hello members,

This chain will bring about how to do basic diagnosis of various cases. It will be as follows:

  • The participant will solve the case and spot the diagnosis.
  • He/she will add another case for the next participant.
  • The case can comprise of photograph to identify it.
  • It can be the clinical features or an investigations.

I hope this chain will be as useful as the previous blog 'Word game in Homoeopathy".

 

Thanks and regards,

Nilanjana

 

Note: This blog will only be for diagnosis.

 

To start with, This is a photograph. Please identify what is the illness she is suffering from?

 

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Comment by Nilanjana Basu on January 10, 2011 at 3:58am
Dear members, please follow the above link to answer.
Comment by Dr Ravindra Saraswat on January 9, 2011 at 11:19am

Dr Vikas-

Duchenne's MuscularDystrophy is a condition that involves wasting of muscles and is hereditary in nature. It is a linked disorder wherein the mother is the carrier. Males are affected. The Duchenne type affects only boys (with extremely rare exceptions) and a problem in this gene is known to result in a defect in a single important protein in muscle fibres called dystrophin. Doctors are also working on improving muscle and joint function, and slowing muscle deterioration so that kids, teens, and adults with MD can live as actively and independently as possible.

Duchenne muscular dystrophy is an inherited disorder, characterized by rapidly-worsening muscle weakness that starts in the legs and pelvis, and later affects the whole body. DMD is one of the most prevalent types of muscular dystrophy and is characterized by rapid progression of muscle degeneration that occurs early in life. This makes the muscle cells weak and they gradually break down. A child who is diagnosed with MD gradually loses the ability to do things like walk, sit upright, breathe easily, and move the arms and hands. DMD is named after the French neurologist Guillaume Benjamin Amand Duchenne (1806-1875), who first described the disease in the 1860s. It is due to mutations in the dystrophin gene, which encodes a cell membrane protein in myocytes (muscle cells). Signs of weakness start when the boys are between 3 and 5 years of age (sometimes earlier).

Comment by Nilanjana Basu on January 8, 2011 at 3:13am
Comment by Nilanjana Basu on January 8, 2011 at 3:00am

Dear all,

Debby and I decided to have this topic in forum Discussion so that there can be more comments and threads which can be edited by you, too. So, please click on the link below to reach the discussion.

Thank you so much, inconvience regretted.

 

Nilanjana

 

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