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.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.uri |
http://hdl.handle.net/11616/47316 |
|
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.language.iso |
eng |
en_US |
dc.relation.isversionof |
10.5455/jtomc.2016.12.126 |
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 |
dc.relation.journal |
Annals of Medical Research |
en_US |
dc.contributor.department |
İnönü Üniversitesi |
en_US |