Literature DB >> 8506220

Complex mosaicism associated with trisomy 9.

J S Smoleniec1, T Davies, P Lunt, P J Berry, D James.   

Abstract

Fetal karyotypes can be routinely obtained by chorionic villus biopsy, amniocentesis, or fetal blood sampling. Interpretation of results and subsequent counselling can be complicated by pseudomosaicism or mosaicism confined to the placenta or other tissues. We illustrate this by reporting a case of an abnormal fetus with a total of three karyotypically different cell lines (46,XX; 47,XX, +9; and 47,XX, +del(9) (q11) in different tissues (placenta, lung, gonad, and skin).

Mesh:

Year:  1993        PMID: 8506220     DOI: 10.1002/pd.1970130308

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


  2 in total

1.  Trisomy 9 mosaicism diagnosed in utero.

Authors:  Hironori Takahashi; Satoshi Hayashi; Yumiko Miura; Keiko Tsukamoto; Rika Kosaki; Yushi Itoh; Haruhiko Sago
Journal:  Obstet Gynecol Int       Date:  2010-07-25

2.  Birth of a child with trisomy 9 mosaicism syndrome associated with paternal isodisomy 9: case of a positive noninvasive prenatal test result unconfirmed by invasive prenatal diagnosis.

Authors:  Jingmei Ma; David S Cram; Jianguang Zhang; Ling Shang; Huixia Yang; Hong Pan
Journal:  Mol Cytogenet       Date:  2015-06-26       Impact factor: 2.009

  2 in total

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