Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
Identifieur interne : 005D66 ( Ncbi/Curation ); précédent : 005D65; suivant : 005D67Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
Auteurs : Z. Cetin [Turquie] ; I. Mendilcioglu [Turquie] ; S. Yakut [Turquie] ; S. Berker-Karauzum [Turquie] ; B. Karaman [Turquie] ; G. Luleci [Turquie]Source :
- Balkan Journal of Medical Genetics : BJMG [ 1311-0160 ] ; 2011.
Abstract
We present here a 16-year-old Turner syndrome patient with a complex karyotype that includes a maternally-inherited balanced translocation between chromosomes 4 and 16 and mosaicism of the isochromosome Xq10. Her karyotype was 45,X,t(4;16) (p15.2;p13.1)[
Url:
DOI: 10.2478/v10034-011-0019-y
PubMed: 24052704
PubMed Central: 3776687
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)</title>
<author><name sortKey="Cetin, Z" sort="Cetin, Z" uniqKey="Cetin Z" first="Z" last="Cetin">Z. Cetin</name>
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<author><name sortKey="Mendilcioglu, I" sort="Mendilcioglu, I" uniqKey="Mendilcioglu I" first="I" last="Mendilcioglu">I. Mendilcioglu</name>
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<author><name sortKey="Berker Karauzum, S" sort="Berker Karauzum, S" uniqKey="Berker Karauzum S" first="S" last="Berker-Karauzum">S. Berker-Karauzum</name>
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<author><name sortKey="Karaman, B" sort="Karaman, B" uniqKey="Karaman B" first="B" last="Karaman">B. Karaman</name>
<affiliation wicri:level="1"><nlm:aff id="af3-bjmg-14-01-57">Prenatal Diagnosis Centre, Faculty of Medicine, Istanbul University, Istanbul, Turkey</nlm:aff>
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<author><name sortKey="Luleci, G" sort="Luleci, G" uniqKey="Luleci G" first="G" last="Luleci">G. Luleci</name>
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<front><div type="abstract" xml:lang="en"><p>We present here a 16-year-old Turner syndrome patient with a complex karyotype that includes a maternally-inherited balanced translocation between chromosomes 4 and 16 and mosaicism of the isochromosome Xq10. Her karyotype was 45,X,t(4;16) (p15.2;p13.1)[<xref ref-type="bibr" rid="b9-bjmg-14-01-57">9</xref>
]/46,X,i(X) (q10),t(4;16)(p15.2;p13.1) [91]. The karyotype of her father was normal, whereas that of her mother had the same balanced translocation and numerical abnormalities of chromosome X and was designated as 45,X,t(4;16)(p15.2;p13.1) [2]/46,XX,t(4;16)(p15.2;p13.1)[93]/47,XXX,t(4;16) (p15.2; p13.1)[<xref ref-type="bibr" rid="b5-bjmg-14-01-57">5</xref>
]. The two siblings of the patient also had the same reciprocal translocation. We consider this to be the first such patient with an inherited reciprocal translocation and structural abnormality of the X chromosome (isochromosome Xq).</p>
</div>
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