Literature DB >> 6353401

Prenatal detection of hydrolethalus syndrome.

A L Hartikainen-Sorri, P Kirkinen, R Herva.   

Abstract

The prenatal diagnosis of hydrolethalus syndrome is presented on the basis of seven cases. The results demonstrate the primary importance of ultrasonography in the evaluation of this type of malformation. Already in early pregnancy, the intracranial abnormalities and the accelerated growth rate of the fetal head are demonstrable by ultrasound more easily than in ordinary 'simple' hydrocephalus. Diagnostic amniocentesis in early pregnancy proved to be useless because alpha-fetoprotein levels and chromosomal status were normal.

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Year:  1983        PMID: 6353401     DOI: 10.1002/pd.1970030306

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  3 in total

1.  Hydrolethalus syndrome.

Authors:  R Salonen; R Herva
Journal:  J Med Genet       Date:  1990-12       Impact factor: 6.318

2.  Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25.

Authors:  I Visapää; R Salonen; T Varilo; P Paavola; L Peltonen
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

3.  Prenatal diagnosis of a probable hereditary syndrome with holoprosencephaly, hydrocephaly, octodactyly, and cardiac malformations.

Authors:  W Grote; H Rehder; D Weisner; H R Wiedemann
Journal:  Eur J Pediatr       Date:  1984-12       Impact factor: 3.183

  3 in total

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