Literature DB >> 2626411

A rare case of 68,XX triploidy diagnosed by amniocentesis.

S Kaffe1, C Eliasen, L Wan, N Charles, V Jansen, M A Greco, L Y Hsu.   

Abstract

68,XX triploidy was found in the amniotic fluid cell culture of a 40-year-old patient. Elective termination of the pregnancy revealed a fetus with multiple congenital anomalies. While this case does show some common features with monosomy X, a greater similarity to the triploidy syndrome is observed.

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Year:  1989        PMID: 2626411     DOI: 10.1002/pd.1970091206

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


  1 in total

1.  Phenotypic expression of the first liveborn 68,XX triploid newborn.

Authors:  P Merlob; N Naor; M Shohat
Journal:  J Med Genet       Date:  1991-12       Impact factor: 6.318

  1 in total

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