Literature DB >> 18395875

Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage.

M T M Franssen1, J C Korevaar, W M Tjoa, N J Leschot, P M M Bossuyt, A C Knegt, R F Suykerbuyk, R Hochstenbach, F van der Veen, M Goddijn.   

Abstract

OBJECTIVE: To determine the mode of ascertainment of inherited unbalanced structural chromosome abnormalities detected at prenatal chromosome analysis.
METHODS: From the databases of three centres for clinical genetics in the Netherlands, all cases of inherited unbalanced structural chromosome abnormalities detected at prenatal chromosome analysis in the period 1992-2000 were selected. The mode of ascertainment was identified by examining the reason for prenatal chromosome analysis and the reason for parental chromosome analysis of the first structural chromosome abnormality detected within the family.
RESULTS: Totally 56 cases of inherited unbalanced structural chromosome abnormalities were detected at prenatal chromosome analysis. Only one case was ascertained through two previous miscarriages (2%). The main modes of ascertainment were a previous child with an unbalanced karyotype (48%), congenital abnormalities at ultrasound examination (20%), and advanced maternal age (9%). The remaining cases had a different mode of ascertainment.
CONCLUSION: Inherited unbalanced structural chromosome abnormalities detected at prenatal chromosome analysis are rarely ascertained through two or more miscarriages. 2008 John Wiley & Sons, Ltd

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Year:  2008        PMID: 18395875     DOI: 10.1002/pd.1960

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


  3 in total

1.  Prenatal Diagnosis of Rare Familial Unbalanced Translocation of Chromosomes 7 and 12.

Authors:  Berrin Tezcan; Foteini Emmanouella Bredaki
Journal:  Case Rep Obstet Gynecol       Date:  2015-07-30

2.  Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia.

Authors:  Rola F Turki; Mourad Assidi; Huda A Banni; Hanan A Zahed; Sajjad Karim; Hans-Juergen Schulten; Muhammad Abu-Elmagd; Abdulrahim A Rouzi; Osama Bajouh; Hassan S Jamal; Mohammed H Al-Qahtani; Adel M Abuzenadah
Journal:  BMC Med Genet       Date:  2016-10-10       Impact factor: 2.103

3.  Association of heteromorphism of chromosome 9 and recurrent abortion (ultrasound diagnosed blighted ovum): A case report.

Authors:  Fatemeh Baghbani; Salmeh Mirzaee; Mohammad Hassanzadeh-Nazarabadi
Journal:  Iran J Reprod Med       Date:  2014-05
  3 in total

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