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4.
Klin Padiatr ; 200(6): 457-62, 1988.
Article in German | MEDLINE | ID: mdl-2907063

ABSTRACT

This is a case-report of a male infant with typical signs of Cornelia de Lange syndrome. Coordination to subtype I or II of the disease is difficult, as somatical and intracerebral dysplasia (partial cerebellar aplasia) are combined. The etio-pathogenetic back-ground and the symptoms of the disorder will be discussed. Finally we point out to a omnidirectional therapeutic concept including several surgical and nonsurgical disciplines with the aim, to make life as easy as possible for these children.


Subject(s)
De Lange Syndrome/surgery , Patient Care Team , Referral and Consultation , Cleft Palate/surgery , Combined Modality Therapy , Cryptorchidism/surgery , De Lange Syndrome/diagnosis , De Lange Syndrome/genetics , Hernia, Inguinal/surgery , Humans , Infant, Newborn , Male , Tomography, X-Ray Computed
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