The FGG c.952G > A variant causes congenital dysfibrinogenemia characterized by recurrent cerebral infarction: a case report
ConclusionThis case report expands the clinical phenotype spectrum associated with FGG c.952G>A (rs267606810) and underscores the significance of considering CD as a potential etiology for unexplained ischemic stroke, particularly in patients with a family history of coagulation disorders.
Source: Frontiers in Neurology - Category: Neurology Source Type: research
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