TY  - JOUR 
TI  - Meckel syndrome with omphalocele and cleft lip
PB  - Editorial Ciencias Medicas
PY  - 2014
issn 0138-600X
AB  - 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.

KW  - Defectos congénitos
KW  - Encefalocele
KW  - Ciencias  socio biomédicas
KW  - Medical sciences
UR  - http://hdl.handle.net/10906/81226
ER  -