Turner syndrome and morgagni hernia in newborn: A case report

Abstract

Turner syndrome is identified by the combination of a number of phenotypic findings at birth as lymphedema of hands and feet, “pterygium colli,” shield chest, congenital cardiopathy, and characteristic morphological data birth whose etiology is supported in the cytogenetic study that determines the total absence of an X chromosome, monosomy of chromosome X, (45, X), identified in 40-60% of cases. It is one of the most frequent chromosomal abnormalities. Congenital diaphragmatic hernia (CDH) is a common birth defect. 2% occur in the anterior Morgagni orifice, the etiology of the majority of the cases remains unknown, but there is growing evidence of genetic causation, the data are supported by the association with recurrent chromosomal abnormalities and the existence of multiple transmission families of CDH; however, there are not many records in association with total or partial monosomy of chromosome X, reason for this report