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Familial atypical hemolytic uremic syndrome with positive p.S1191L (c.3572C>T) mutation on the CFH gene: A single-center experience Cover

Familial atypical hemolytic uremic syndrome with positive p.S1191L (c.3572C>T) mutation on the CFH gene: A single-center experience

Balkan Journal of Medical Genetics
Volume 24 (2021): Issue 1 (June 2021)
By: F Ersoy Dursun,  G Yesil,  G Sasak and  H Dursin  
Open Access
|Jul 2021

Authors

F Ersoy Dursun

drfadimeersoy@yahoo.com.tr

Department of Hematology, Medeniyet University, Goztepe Training and Research Hospital, Istanbul, Turkey

G Yesil

Department of Medical Genetics, Bezmialem Vakif University, School of Medicine, Istanbul, Turkey

G Sasak

Department of Nephrology, Medeniyat University, Goztepe Training and Research Hospital, Istanbul, Turkey

H Dursin

Department of Pediatric Nephrology, Istanbul Health Sciences University, Okmeydani Training and Research Hospital, Istanbul, Turkey
DOI: https://doi.org/10.2478/bjmg-2021-0007 | Journal eISSN: 2199-5761
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Language: English
Page range: 81 - 88
Published on: Jul 27, 2021
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Complement factor H () gene,
Eculizumab (ECZ),
Familial atypical hemolytic uremic syndrome (aHUS),
Plasmapheresis,
p.S1191L mutation
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2021 F Ersoy Dursun, G Yesil, G Sasak, H Dursin, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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