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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Detalles Bibliográficos
Autores principales: Hassan, Abdulaziz, Adebayo, Adeshola, Musa, Abubakar Umar, Suleiman, Aishatu Maude, Ibrahim, Ismaila Nda, Kusfa, Ibrahim Usman, Aminu, Mohammed Sirajo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726176/
https://www.ncbi.nlm.nih.gov/pubmed/29269984
http://dx.doi.org/10.4103/0300-1652.219343

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726176/
https://www.ncbi.nlm.nih.gov/pubmed/29269984
http://dx.doi.org/10.4103/0300-1652.219343

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