Marfan syndrome: A case report with review of literature
| dc.contributor.author | Castelino, Renita Lorina | |
| dc.contributor.author | Ka, Fazil | |
| dc.contributor.author | Babu, Subhas G | |
| dc.contributor.author | Balan, Preethi | |
| dc.contributor.author | Bhat, Supriya | |
| dc.date.accessioned | 2022-02-16T13:11:14Z | |
| dc.date.available | 2022-02-16T13:11:14Z | |
| dc.date.issued | 2017 | |
| dc.department | İnönü Üniversitesi | en_US |
| dc.description.abstract | Marfan syndrome is a systemic condition involving the connective tissue. The syndrome is inherited by autosomal dominant trait. Affected persons carry a mutation in the gene that encodes fibrillin-1 which is a connective tissue protein. The incidence of this syndrome is one in ten thousand live births with an equal predilection for both the genders. The syndrome is a collection of generalized manifestations involving the skeleton, eyes, heart, lungs, and the large blood vessels. The individual affected by this syndrome is usually tall and lean with various systemic abnormalities. A case of Marfan syndrome is reported here with review of literature. | en_US |
| dc.identifier.citation | Ka, F., Lorina Castelino, R., Babu, S., Balan, P., & Bhat, S. (2021). Marfan syndrome: A case report with review of literature . Annals of Medical Research, | en_US |
| dc.identifier.doi | 10.5455/jtomc.2016.12.126 | en_US |
| dc.identifier.uri | https://hdl.handle.net/11616/47316 | |
| dc.language.iso | en | en_US |
| dc.relation.ispartof | Annals of Medical Research | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Marfan syndrome: A case report with review of literature | en_US |
| dc.type | Article | en_US |
