Literature DB >> 1583306

[Complete and homogenous trisomy 9 detected in utero].

F Raffi1, A Geneix, D Satge, B Fallouh, A M Brunerie, D Lemery, P Malet.   

Abstract

During a gestation with oligoamnios and growth retardation noticed at 25th week an amniocentesis allowed us to discover the 14th case of complete trisomy 9, the third detected in utero. It is also the first without heart malformation, otherwise phenotype was usual. The liver had small areas of necrosis with calcifications and slight fibrosis which may be in relation with two cordocentesis made before expulsion. The important phenotype alterations and poor outcome of fetuses with trisomy 9 justify elective abortion.

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Year:  1992        PMID: 1583306

Source DB:  PubMed          Journal:  J Gynecol Obstet Biol Reprod (Paris)        ISSN: 0150-9918


  1 in total

Review 1.  Trisomy 9 mosaicism in two girls with multiple congenital malformations and mental retardation.

Authors:  C Stoll; D Chognot; A Halb; J C Luckel
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318

  1 in total

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