Talk:Spherocytosis

Hereditary spherocytosis

A lot of the material here is redundant with hereditary spherocytosis. This article should focus on the differential diagnosis of spherocytes on the peripheral blood smear. JFW | T@lk 09:45, 23 October 2005 (UTC)

I would suggest at least merging the information in the hereditary spherocytosis article that applies more generally into this article. For example, the symptoms for both should fall within the general category of symptoms of spherocytosis, whereas symptoms specific to hereditary spherocytosis should appear only in that article. --ojo 2006-01-03@21h58m(UTC)

I've edited for the causes (found in a book) and for the definition. Hope it's clearer! — Preceding unsigned comment added by Linuxo (talk • contribs) 10:13, 21 May 2018 (UTC)

Workplan for Spherocytosis

Workplan as follows:

   Provide source material updates.
   Provide citations where missing.
   Recreate a more formal lead section.
   Reorganize the article to correspond to the structure provided by the lead section, which will tie the article closer to the more frequently searched Hereditary Spherocytosis.
   Adjust the sections to follow standard medical encyclopedia formatting.
   Add information in all sections to ensure that a reader could master the entirety of the topic from studying this article.
   Prioritization will be given to differential diagnosis.

Gensurg22 (talk) 22:38, 19 March 2022 (UTC)