Síndrome de Meckel con onfalocele y labio fisurado / Meckel syndrome with omphalocele and cleft lip
Rev. cuba. obstet. ginecol
; 40(2): 272-278, abr.-jun. 2014.
Article
in Spanish
| LILACS
| ID: lil-717229
Responsible library:
CU1.1
RESUMEN
El síndrome de Meckel es un desorden autosómico recesivo, raro y letal. Se caracteriza por múltiples malformaciones, entre estas, la triada de encefalocele occipital, riñones poliquísticos y polidactilia. Se presenta un caso con múltiples malformaciones incluyendo las menos frecuentes como el onfalocele, la hipospadia y el labio fisurado.
ABSTRACT
The Meckel Gruber syndrome is a lethal, rare and autosomal disorder. It is characterized by multiple malformations, among these the triad of occipital encephalocoele, large polycystic kidneys and post-axial polydactyly. A case with multiple malformations, including the less frequent as omphalocele, hypospadias and cleft lip is presented.
Full text:
Available
Collection:
International databases
Database:
LILACS
Language:
Spanish
Journal:
Rev. cuba. obstet. ginecol
Journal subject:
Gynecology
/
Obstetrics
Year:
2014
Document type:
Article
Affiliation country:
Colombia
Institution/Affiliation country:
Universidad Icesi/CO