Marfan syndrome affecting a whole Sudanese family.

Laila M Elmahdi; Sulafa Km Ali

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Sudan J Paed. 2013; 13(1): 53-5

Marfan syndrome affecting a whole Sudanese family.

Laila M Elmahdi; Sulafa Km Ali.

Abstract
Marfan syndrome (MS, OMIM 154700) is an autosomal dominant disorder of fibrous connective tissue with striking pleiotropism and clinical variability. The cardinal features occur in skeletal, ocular, and cardiovascular systems. We describe a Sudanese family with the father and all his 4 children manifesting the syndrome. To our knowledge, there were no previously reported MS cases from Sudan.

Key words: Echocardiography; Fibrillin-1 gene; Marfan syndrome

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Pubmed Style

Elmahdi LM, Ali SK. Marfan syndrome affecting a whole Sudanese family.. Sudan J Paed. 2013; 13(1): 53-5.

Web Style

Elmahdi LM, Ali SK. Marfan syndrome affecting a whole Sudanese family.. https://sudanjp.com//?mno=280732 [Access: June 21, 2024].

AMA (American Medical Association) Style

Elmahdi LM, Ali SK. Marfan syndrome affecting a whole Sudanese family.. Sudan J Paed. 2013; 13(1): 53-5.

Vancouver/ICMJE Style

Elmahdi LM, Ali SK. Marfan syndrome affecting a whole Sudanese family.. Sudan J Paed. (2013), [cited June 21, 2024]; 13(1): 53-5.

Harvard Style

Elmahdi, L. M. & Ali, . S. K. (2013) Marfan syndrome affecting a whole Sudanese family.. Sudan J Paed, 13 (1), 53-5.

Turabian Style

Elmahdi, Laila M, and Sulafa Km Ali. 2013. Marfan syndrome affecting a whole Sudanese family.. Sudanese Journal of Paediatrics, 13 (1), 53-5.

Chicago Style

Elmahdi, Laila M, and Sulafa Km Ali. "Marfan syndrome affecting a whole Sudanese family.." Sudanese Journal of Paediatrics 13 (2013), 53-5.

MLA (The Modern Language Association) Style

Elmahdi, Laila M, and Sulafa Km Ali. "Marfan syndrome affecting a whole Sudanese family.." Sudanese Journal of Paediatrics 13.1 (2013), 53-5. Print.

APA (American Psychological Association) Style

Elmahdi, L. M. & Ali, . S. K. (2013) Marfan syndrome affecting a whole Sudanese family.. Sudanese Journal of Paediatrics, 13 (1), 53-5.

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