The FGG c.952G>A variant causes congenital dysfibrinogenemia characterized by recurrent cerebral infarction: a case report

The FGG c.952G>A variant causes congenital dysfibrinogenemia characterized by recurrent cerebral infarction: a case report

BackgroundCongenital dysfibrinogenemia (CD) is a rare hereditary coagulation disorder resulting from mutations in fibrinogen genes. CD primarily presents with bleeding symptoms, but it can also lead to thrombotic events, including ischemic stroke.Case presentationThis report describes the case of a...

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Bibliographic Details
Main Authors: Anna Ying, Yuanlin Zhou, Chunyue Wang, Tao Wang, Xuan Zhang, Shanshan Wang, Shaofa Ke, Yuyan Bao, Yang Liu, Feng Wang
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-01-01
Series:Frontiers in Neurology
Subjects:
FGG gene
c.952G>A
congenital dysfibrinogenemia
cerebral infarction
fibrinogen
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2024.1272802/full

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https://www.frontiersin.org/articles/10.3389/fneur.2024.1272802/full

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