Resumen

MEDINA, María Lucia; SALDARRIAGA, Wilmar; ISAZA, Carolina  y  PACHAJOA, Harry. Meckel syndrome with omphalocele and cleft lip. Rev Cubana Obstet Ginecol [online]. 2014, vol.40, n.2, pp. 272-278. ISSN 0138-600X.

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.

Palabras clave : birth defect; polydactyly; encephalocele.

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