Smith-McCort variant syndrome: A rare case with associated enamel hypoplasia

• Asıl Yazarlar: Sandeepa Nuchilakath (Yazar), Jaishankar Homberhalli Puttabuddi (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Wolters Kluwer Medknow Publications, 2015-01-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

The Smith-McCort syndrome (SMC), which was first described by Smith and McCort in 1958, is a rare form of osteochondrodysplasia, specifically a spondyloepimetaphyseal dysplasia. It is one of the rare syndromes that can present with skeletal dysplasia and mimic some of the common bone diseases. Ename...