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...

Full description

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/
Description
Summary: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 omphalocele, hypospadias and cleft lip is presented.