%0 Case Reports
%T A Forme Fruste of Marfan Syndrome: A Case Report.
%A Alsheikh N
%A Hawsawi SA
%A AlGhamdi A
%A Alkhwaiter L
%A Alsulimani A
%A Suliman I
%J Cureus
%V 14
%N 11
%D Nov 2022
%M 36505128
暂无%R 10.7759/cureus.31231
%X Marfan syndrome (MFS), an inherited connective tissue disorder, is caused by a mutation in the FBN1 gene. MFS is characterized by manifestations in the musculoskeletal system (joint laxity, scoliosis), the cardiovascular system (aortic dilation), and the ocular system (ectopic lens). We report a case of a 37-year-old male with a genetically confirmed MFS. His mother and brother were also both confirmed cases of MFS. While the patient exhibited the characteristic physical features of MFS in general appearance, he did not show any cardiac manifestations of the disease. This report highlights a case of the familial occurrence of MFS and emphasizes the importance of recognizing the forme fruste of MFS.