|Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Iron overload.
|WikiProject Medicine / Pathology||(Rated C-class, Mid-importance)|
Mention DNA testing
Add reference explaining "type 1" and "type 2"
Does anyone know what those "type 1" "type 2" etc are referring to? I can't find references to those, so I'm not sure if those are standard or accepted terms. If they're not verifiable, they may need to be deleted. --Arcadian 00:51, 1 December 2005 (UTC)
- Look at the Pietrangelo article, where I based this list on. It's not in common use and may be deleted. JFW | T@lk 01:27, 1 December 2005 (UTC)
- Thanks -- that was what I was looking for. I've added the OMIM codes to the "Primary iron overload" section, but I've got a question -- we have one entry for "Type 2: Juvenile hereditary iron overload" and another entry for "Juvenile haemochromatosis". Are they the same thing, or distinct conditions? For now, I listed them both with the same OMIM code. --Arcadian 14:03, 8 December 2005 (UTC)
- Oh no. I'm not sure now. I have no access to Gut anymore to double-check the Pietrangelo article. JFW | T@lk
under the heading, Terminology, prevalence and incidence should not be used interchangeably. These terms have different mathematical definitions, with incidence being commonly used to describe the risk of a new case in an individual who is not already known to have the condition, while prevalence describes the disease burden in the population at large. — Preceding unsigned comment added by 126.96.36.199 (talk) 10:22, 30 June 2011 (UTC)
Genetic testing in families to screen for preventitive measures
Is there a good way to mention genetic testing for families that have one member diagnosed with type 1 for preventative medicine? I am asking because this testing has saved many menbers of my familys lives, especially those not yet presenting symproms, they can limit their iron intake to prevent organ damage. Please advise. 188.8.131.52 (talk) 16:22, 30 October 2011 (UTC)
"Although hereditary Hemochromatosis varies in clinical severity, the most common presenting feature is fatigue." Lyon E, Frank EL. Clinical Chemistry July 2001 vol. 47 no. 7 1147-1156
This is also repeated liberally elsewhere in many respected peer-reviewed sources relating to hemochromatosis.
HFE protein, or HFE gene?
Text itself should specify whether gene or protein is meant -- just "HFE" is patently ambiguous.
In any case, "HFE" is jargon not understood by the vast majority of English readers, and failure to specify and provide the words for which the initials stand makes the article unnecessarily opaque. — Preceding unsigned comment added by 184.108.40.206 (talk) 19:33, 30 June 2013 (UTC)
Signs and symptoms
Devanshuv added content about the signs and symptoms of iron overload. Most of the sources, however, don't talk about ironload as a whole but specifically about HFE gene haemochromatosis. People with transfusional iron overload have another phenotype altogether. I think we should stick to a single source that is clearly about all types of iron overload, or a source that delineates whether a sign or symptom is typical for haemochromatosis or all types. JFW | T@lk 19:44, 8 April 2014 (UTC)
- Thanks Jfdwolff for pointing that out. I agree most signs and symptoms were associated with HFE gene hemochromatosis as a cause. One potential source that delineates signs and symptoms typical for all types may include Review article: the iron overload syndromes. An idea open for discussion could also include creating a table with the rows as the organ systems and the columns as the different syndromes. A rough example might look like:
|Cause 1||Cause 2||Cause 3|