Difference between revisions of "Talk:Hemochromatosis 2012"

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=== Content ===
 
=== Content ===
* Section '''Summary''': Though this site focuses on hereditary hemochromatosis (hemochromatosis type 1) it is worth noting, that there are differrent types of hemochromatosis.
 
Did you mean:
 
Though this site focuses on hereditary hemochromatosis (hemochromatosis type 1) it is worth '''mentioning''', that there are different types of hemochromatosis.[Julia]
 
 
* Section '''Summary''': Because the accumulation of iron is a slow process most patients show symptoms between the age of 30 to 60.
 
* Section '''Summary''': Because the accumulation of iron is a slow process most patients show symptoms between the age of 30 to 60.
 
They appear for the first time at this age, don't they? It sounds as if they would only show until you are 60... In section '''Phenotype''' you write:
 
They appear for the first time at this age, don't they? It sounds as if they would only show until you are 60... In section '''Phenotype''' you write:

Latest revision as of 13:22, 21 February 2013

Feedback

I really like your wiki, I think it is clear and brief. Though, I have a couple of notes.

Formal

  • Maybe you should try starting less sentences with "Hereditary hemochromatosis ..." [Julia]
  • In Reference Sequence, I like that you highlighted the positions of known mutations in red. [Julia]
  • It might be helpful for the reader if you refer to the pictures at the proper place in the text. Especially for the figures "iron absorption pathway" and "HFE mutation effects". [Julia]

Content

  • Section Summary: Because the accumulation of iron is a slow process most patients show symptoms between the age of 30 to 60.

They appear for the first time at this age, don't they? It sounds as if they would only show until you are 60... In section Phenotype you write: Most patients begin to show symptoms between the age of 30 and 60. Maybe this wording is better.[Julia]