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Pediatr Med Chir ; 19(2): 117-9, 1997.
Article in Italian | MEDLINE | ID: mdl-9312746

ABSTRACT

Defects of the middle line are an heterogeneous group of congenital malformations due to commune pathogenetic mechanisms. We have made a case-control study about 150 newborns, who have at least 1 defect of the middle line. Results prove an excess of males between the cases, due mostly to hypospadias. We haven't found families with defects of the middle line with x-linked manner of hereditary transmission. We haven't found any particular risk present in cases and not in controls. We haven't found any case with 2 or more middle line defects.


Subject(s)
Congenital Abnormalities/genetics , Case-Control Studies , Cleft Lip/genetics , Cleft Palate/genetics , Esophageal Atresia/genetics , Esophageal Fistula/genetics , Female , Gestational Age , Humans , Hypospadias/genetics , Infant, Newborn , Male , Sex Factors , Trachea/abnormalities
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