A rare sporadic case of C3 gene mutation in 5-month-old baby girl with atypical hemolytic uremic syndrome, with good prognosis

A rare sporadic case of C3 gene mutation in 5-month-old baby girl with atypical hemolytic uremic syndrome, with good prognosis

Atypical hemolytic uremic syndrome (aHUS) is a rare form of thrombotic microangiopathy representing <10% of HUS cases, characterized by hemolytic anemia, thrombocytopenia, and renal failure. A 5-month-old baby girl, the daughter of Saudi nonconsanguineous parents, presented with fever, vomiting,...

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Bibliographic Details
Main Authors: Abdullah A Baothman, Hani Almalki, Mohammed Almaghrabi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Journal of Applied Hematology
Subjects:
Atypical hemolytic uremic syndrome
eculizumab
microangiopathy
Online Access:http://www.jahjournal.org/article.asp?issn=1658-5127;year=2018;volume=9;issue=3;spage=104;epage=107;aulast=Baothman

Internet

http://www.jahjournal.org/article.asp?issn=1658-5127;year=2018;volume=9;issue=3;spage=104;epage=107;aulast=Baothman

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