A Rare De Novo Robertsonian Translocation 45, XX, rob (13;13) (q10; q10) Karyotype Carrying in a Normal Woman; But Recurrent Abortions
نویسندگان
چکیده
The most common cause of pregnancy losses is chromosomal anomalies. Fetal chromosomal anomalies are found in 90% preembryonic losses, 50% first trimester abortions, 2/3 malformed embryos, and 1/3 malformed fetuses. Considering all pregnancy losses, the rate 50%...
منابع مشابه
A Robertsonian Translocation rob (14;15) (q10:q10) in a Patient with Recurrent Abortions: A Case Report
INTRODUCTION Robertsonian translocation is one of the major chromosomal rearrangements with a prevalence rate of 0.1% of the general population and 1% of the infertile population. In this report, we present a nonhomologous Robertsonian translocation in a female patient with a history of repeated abortions. CASE PRESENTATION A couple with the complaint of repeated abortions was admitted in the...
متن کاملa robertsonian translocation rob (14;15) (q10:q10) in a patient with recurrent abortions: a case report
introduction: robertsonian translocation is one of the major chromosomal rearrangements with a prevalence rate of 0.1% of the general population and 1% of the infertile population. in this report, we present a nonhomologous robertsonian translocation in a female patient with a history of repeated abortions. case presentation: a couple with the complaint of repeated abortions was admitted in the...
متن کاملA 21/22 Translocation in a Female with Repeated Abortions: A Case Report
Robertsonian translocations (RT’s) are present in 0.1% of the general population and 1% of the infertile population. Two types of RT’s occur more frequently than all others, being 45,XX,rob(13;14)(q10;q10) and 45,XX,rob(14;21)(q10;q10) respectively. In the present report, an uncommon RT in a female with spontaneous repeated abortions is reported. Cytogenetic analysis of a couple with repeated a...
متن کاملSperm FISH studies in seven male carriers of Robertsonian translocation t(13;14)(q10;q10).
BACKGROUND Robertsonian translocation t(13;14) is one of the most common structural reorganization in humans, but meiotic segregation studies in these carriers are still limited. The segregation pattern of the chromosomes involved, the possible influence of the translocated chromosomes on the synapsis and disjunction of other chromosome pairs [interchromosomal effects (ICE)] and the rates of un...
متن کاملVarious endocrine disorders in children with t(13;14)(q10;q10) Robertsonian translocation
PURPOSE 45,XY,t(13;14)(q10;q10) karyotype can suggest infertility associated with more or less severe oligospermia in male adults. In addition, 45,XX,t(13;14)(q10;q10) karyotype carries reproductive risks such as miscarriage or infertility in female adults. However, reports on the phenotype of this karyotype in children are very rare. This study was done to observe various phenotypes of this ka...
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ژورنال
عنوان ژورنال: Biomedical Journal of Scientific and Technical Research
سال: 2021
ISSN: ['2574-1241']
DOI: https://doi.org/10.26717/bjstr.2021.36.005783