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Hemoglobin Sickle Cell Disease and Systemic Lupus Erythematosus

An unusual association of hemoglobin sickle cell disease with systemic lupus erythematosus in an 11-year-old girl highlights the diagnostic dilemma that may arise because of the similarity of symptomatology.

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Bibliografiske detaljer
Main Authors: Warrier, R.P., Sahney, S., Walker, H.
Format: Artigo
Sprog:Inglês
Udgivet: 1984
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2561782/
https://ncbi.nlm.nih.gov/pubmed/6502719
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