Cargando…
Ellis-van Creveld syndrome in an Indian child: a case report
Ellis-van Creveld syndrome is a rare congenital genetic disorder having autosomal recessive inheritance. It is a syndrome affecting the Amish population of Pennsylvania in USA with prevalence rate of 1/5,000 live at birth. In non-Amish population, the birth prevalence is 7/1,000,000. The syndrome is...
Autores principales: | Veena, K.M., Jagadishchandra, H., Rao, Prasanna Kumar, Chatra, Laxmikanth |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Oral and Maxillofacial Radiology
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251790/ https://www.ncbi.nlm.nih.gov/pubmed/22232726 http://dx.doi.org/10.5624/isd.2011.41.4.167 |
Ejemplares similares
-
Ellis–van Creveld
por: Jayaraj, Dhandabani, et al.
Publicado: (2012) -
Ellis-Van Creveld syndrome
por: Baujat, Geneviève, et al.
Publicado: (2007) -
Ellis-van Creveld Syndrome: A Case Report
por: Singh, Subash, et al.
Publicado: (2012) -
Oral manifestations of Ellis-van Creveld syndrome
por: Kalaskar, Ritesh, et al.
Publicado: (2012) -
Ellis van Creveld syndrome in a Tunisian child revealed by an Eisenmenger syndrome
por: Ajmi, Houda, et al.
Publicado: (2015)