Literature DB >> 8464840

Prenatal diagnosis of Dandy-Walker malformation in a family displaying X-linked inheritance.

T Cowles1, P Furman, I Wilkins.   

Abstract

The diagnosis of Dandy-Walker malformation was made on the ultrasonographic evaluation of a 33-week male fetus. Pedigree analysis revealed a family history of isolated Dandy-Walker malformation in three other males, suggesting an X-linked recessive inheritance pattern.

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Year:  1993        PMID： 8464840     DOI： 10.1002/pd.1970130203

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


  2 in total

1.  Familial Dandy-Walker syndrome: a case report supporting an autosomal inheritance.

Authors:  Thomas W H Bragg; Edward J St George; Guy A Wynne-Jones; Anthony Hockley; Jenny E V Morton
Journal:  Childs Nerv Syst       Date:  2005-11-01       Impact factor: 1.475

2.  Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion.

Authors:  A Tar; J Sólyom; B Györvári; A Ion; L Telvi; S Barbaux; N Souleyreau; E Vilain; M Fellous; K McElreavey
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132
  2 in total

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