Literature DB >> 302671

Free trisomy 9P in elderly woman.

U Gripenberg, K Hongell, M Iivanainen, T Kivimäki.   

Abstract

The karyotype 47,XX,+9p was observed in a 50-year-old mentally retarded woman with dysmorphic facies, severe cerebral malformations, limb deformities, retarded sexual maturation and deviating dermatoglyphs. Banding analysis showed the extra chromosome to be composed of 9p and the proximal part of 9q comprising a large secondary constriction. The breakage point is estimated as 9q13. Hemozygous large C bands were observed in both chromosomes No. 9 as well as in the extra chromosome. Clinically this case can be regarded as a pure 9p trisomy. The mechanism causing the syndrome is thought to be malsegregation of a deleted chromosome No. 9.

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Year:  1977        PMID: 302671

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  2 in total

1.  Duplication of the short arm of chromosome 9. Analysis of five cases.

Authors:  C Cuoco; G Gimelli; F Pasquali; L Poloni; O Zuffardi; P Alicata; G Battaglino; F Bernardi; R Cerone; M Cotellessa; A Ghidoni; S Motta
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

2.  Partial Trisomy 9p(p22→pter) from a Maternal Translocation 4q35 and 9p22.

Authors:  F Mahjoubi; F Nasiri; R Torabi
Journal:  Balkan J Med Genet       Date:  2011-06       Impact factor: 0.519

  2 in total

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