Literature DB >> 15906424

Prenatal diagnosis of trisomy 6 mosaicism.

A Destree1, C Fourneau, C Dugauquier, S Rombout, D Sartenaer, Y Gillerot.   

Abstract

We report on a fetus with multiple congenital anomalies detected at the prenatal ultrasound examination and a trisomy 6 mosaicism in the amniocytes. The pregnancy was interrupted in the 18th gestational week and the autopsy revealed malformations including cleft right hand, arthrogryposis and hypoplasia of the 4th digit of the left hand, syndactylies and overlapping toes, facial dysmorphism with hypertelorism and low-set ears, ventricular septum defect (VSD), intestinal malrotation and scoliosis. Trisomy 6 mosaicism was detected in cultured amniocytes (13.3%), confirmed in umbilical cord fibroblasts (40%) and by fluorescence in situ hybridization on other fetal tissues. Trisomy 6 mosaicism is a very rare finding with only eight cases previously reported to our best knowledge. Copyright (c) 2005 John Wiley & Sons, Ltd.

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Year:  2005        PMID: 15906424     DOI: 10.1002/pd.1149

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


  3 in total

Review 1.  Arthrogryposis: a review and update.

Authors:  Michael Bamshad; Ann E Van Heest; David Pleasure
Journal:  J Bone Joint Surg Am       Date:  2009-07       Impact factor: 5.284

Review 2.  Constitutional and acquired autosomal aneuploidy.

Authors:  Colleen Jackson-Cook
Journal:  Clin Lab Med       Date:  2011-12       Impact factor: 1.935

3.  Ocular manifestations in Edward's syndrome, a case report and literature review.

Authors:  Arash Mirmohammadsadeghi; Mohammad Reza Akbari; Afsaneh Malekpoor
Journal:  J Curr Ophthalmol       Date:  2017-07-15
  3 in total

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