Clinical feature and management of immune thrombocytopenic purpura in a tertiary hospital in Northwest Nigeria

BACKGROUND: Immune thrombocytopenic purpura (ITP) is a rare bleeding disorder that may remit spontaneously. Life-threatening bleeding may require transfusion support, steroids, and other immunosuppressive therapy or splenectomy. OBJECTIVE: To review the clinical presentation and laboratory features...

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Detaylı Bibliyografya
Yayımlandı:Niger Med J
Asıl Yazarlar: Hassan, Abdulaziz, Adebayo, Adeshola, Musa, Abubakar Umar, Suleiman, Aishatu Maude, Ibrahim, Ismaila Nda, Kusfa, Ibrahim Usman, Aminu, Mohammed Sirajo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2017
Konular:
Original Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5726176/
https://ncbi.nlm.nih.gov/pubmed/29269984
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0300-1652.219343
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