%0 Journal Article 
%T Meckel syndrome with omphalocele and cleft lip
%D 2014
%@ 0138-600X
%U http://hdl.handle.net/10906/81226
%X 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.

%K Defectos congénitos
%K Encefalocele
%K Ciencias  socio biomédicas
%K Medical sciences
%~ GOEDOC, SUB GOETTINGEN