Paroxysmal Nocturnal Hemoglobinuria

dc.contributor.author	Mohamed, Salma Samir
dc.date.accessioned	2019-02-27T09:26:58Z
dc.date.available	2019-02-27T09:26:58Z
dc.date.issued	2018-04-13
dc.identifier.uri	http://repository.limu.edu.ly/handle/123456789/587
dc.description	Paroxysmal Nocturnal Hemoglobinuria is a very rare disease occurs in 1 every million worldwide. It hard to differentiate its symptoms from other overlapping conditions, and takes long time to be properly diagnosed.It is mainly caused by mutation in genes that code anchoring proteins on different blood cells types. The different symptoms mainly depends on intravascular hemolysis. The management aimed to correct the anemia and to prevent life-threatening conditions as thrombi and intravascular clotting	en_US
dc.description.abstract	Paroxysmal Nocturnal Hemoglobinuria originates from mutant genes in stem cells of bone marrow that differentiate to different types of blood cells.Hemolytic anemia, bone marrow failure and thrombophilia is Clinical triad typical for PNH. The management depend on patient case	en_US
dc.language.iso	en	en_US
dc.publisher	faculty of Basic Medical Science - Libyan International Medical University	en_US
dc.rights	Attribution 3.0 United States	*
dc.rights.uri	http://creativecommons.org/licenses/by/3.0/us/	*
dc.title	Paroxysmal Nocturnal Hemoglobinuria	en_US
dc.type	Other	en_US

Except where otherwise noted, this item's license is described as Attribution 3.0 United States