Wiskott–Aldrich syndrome that was initially diagnosed as immune thrombocytopenic purpura secondary to a cytomegalovirus infection

Wiskott–Aldrich syndrome is a rare X-linked recessive disease resulting from variations in the WAS gene. Wiskott–Aldrich syndrome is sometimes difficult to differentiate from immune thrombocytopenic purpura. A 2-month-old boy was admitted to our hospital for purpura and thrombocytopenia. His mean pl...

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Podrobná bibliografie
Vydáno v:SAGE Open Med Case Rep
Hlavní autoři: Kaneko, Ryota, Yamamoto, Shohei, Okamoto, Naoko, Akiyama, Kosuke, Matsuno, Ryosuke, Toyama, Daisuke, Hoshino, Akihiro, Imai, Kohsuke, Isoyama, Keiichi
Médium: Artigo
Jazyk:Inglês
Vydáno: SAGE Publications 2018
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5768273/
https://ncbi.nlm.nih.gov/pubmed/29348920
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2050313X17753788
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