Meckel syndrome with omphalocele and cleft lip
The Meckel Gruber syndrome is a lethal , rare and autosomal disorder. It is characterized by multiple malformation s, among these the triad of occipital encephalocoele, large polycystic kidneys an d post-axial polydactyly. A case with multiple malformations, including the less frequent as omphalocel...
- Autores:
-
Pachajoa Londoño, Harry Mauricio
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2014
- Institución:
- Universidad ICESI
- Repositorio:
- Repositorio ICESI
- Idioma:
- eng
- OAI Identifier:
- oai:repository.icesi.edu.co:10906/81226
- Acceso en línea:
- https://nebulosa.icesi.edu.co/login?url=http://search.ebscohost.com/login.aspx?direct=true&db=edselc&AN=edselc.2-52.0-84905274652&lang=es&site=eds-live&scope=site
http://scielo.sld.cu/pdf/gin/v40n2/gin14214.pdf
http://bvs.sld.cu/revistas/gin/indice.html
http://hdl.handle.net/10906/81226
- Palabra clave:
- Defectos congénitos
Encefalocele
Ciencias socio biomédicas
Medical sciences
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by-nc-nd/4.0/