Open AccessA rare sporadic case of C3 gene mutation in 5-month-old baby girl with atypical hemolytic uremic syndrome, with good prognosis
Author(s) -
Hani Almalki,
AbdullahA Baothman,
Mohammed Almaghrabi
Publication year - 2018
Publication title -
journal of applied hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.107
H-Index - 2
eISSN - 2454-6976
pISSN - 1658-5127
DOI - 10.4103/joah.joah_31_18
Subject(s) - medicine , eculizumab , thrombotic microangiopathy , gastroenterology , pediatrics , peritoneal dialysis , atypical hemolytic uremic syndrome , gene mutation , missense mutation , hemolytic anemia , compound heterozygosity , immunology , mutation , antibody , gene , complement system , biochemistry , chemistry , disease
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