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Marfan syndrome in a Ghanaian male: The diagnostic challenges
Aba A Folson1, Kwabena Oteng Agyapong2, Dzifa Dey3
1Department of Internal Medicine and Therapeutics, School of Medicine University of Health and Allied Sciences Ho Ghana.
Abstract:
Marfan syndrome (MFS) is an autosomal dominantly inherited condition that has varying phenotypic expressions. This case report describes one such African patient, from Ghana, who had typical clinical and imaging traits of MFS but was first diagnosed incidentally at the age of 23 years. In this report, we explore the challenges of early diagnosis in this population.
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