Marfan syndrome: A case report with review of literature
Yükleniyor...
Dosyalar
Tarih
2017
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
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.
Açıklama
Anahtar Kelimeler
Kaynak
Annals of Medical Research
WoS Q DeÄŸeri
Scopus Q DeÄŸeri
Cilt
Sayı
Künye
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,
