Literature DB >> 7710578

Prenatal diagnosis of moderate unilateral hydrocephalus subsequently not requiring neonatal decompression.

D M Sherer1, T A Allen, F Ghezzi, L G Epstein.   

Abstract

Prenatal diagnosis of unilateral hydrocephalus is unusual. In the past most such cases have been treated with neonatal shunting procedures. We present an unusual case in which moderate unilateral hydrocephalus was diagnosed prenatally at 30 weeks' gestation. Despite prenatal and neonatal sonographic signs of both cortical thinning and mild displacement of midline intracranial structures, confirmed by computed tomography, neonatal shunting was not required. The findings and course in this unusual case suggest that infrequently some of the milder cases of idiopathic nonprogressive unilateral hydrocephalus discovered later in life may possibly represent late detection of this preexisting condition.

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Year:  1995        PMID: 7710578     DOI: 10.1055/s-2007-994400

Source DB:  PubMed          Journal:  Am J Perinatol        ISSN: 0735-1631            Impact factor:   1.862


  1 in total

1.  Familial congenital unilateral cerebral ventriculomegaly: Delineation of a distinct genetic disorder.

Authors:  Maha S Zaki; Hanan H Afifi; A J Barkovich; Joseph G Gleeson
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

  1 in total

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