Article
[Ocular manifestations of Marfan syndrome].
Vestnik oftalmologii - 1 Jan 2022
Chizhonkova E A, Avetisov K S, Avetisov S E, Kharlap S I
Abstract excerpt
Marfan syndrome is an orphan disease that is caused by a mutation in the FBN1 gene located on chromosome 15 (15q21.1) and is usually inherited in an autosomal dominant manner. The article reviews the results of studies concerning the potential ocular manifestations of Marfan syndrome. Синдром Марфана — орфанное заболевание, которое вызывается мутацией в расположенном на 15-й хромосоме (15q21.1) гене FBN1 и, как...
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