Literature DB >> 4045963

Complex translocation in a boy with trichorhinophalangeal syndrome.

L M Sánchez, J D Labarta, T C De Negrotti, A M Migliorini.   

Abstract

We report a boy with a trichorhinophalangeal syndrome (TRP syndrome), severe mental retardation, and transient megacephaly, whose karyotype showed complex, apparently balanced, translocations with breakpoints in bands 3q13, 8p22, 8q13, 11p12, and 11q21. The fact that cases presenting with phenotypes corresponding to the TRP II syndrome and deletions of the long arm of chromosome 8 have been recently reported prompted us to report this case to help in the clarification of the possible relation between 8q chromosomal mutation and the aetiology of TRP syndromes.

Entities:  

Mesh:

Year:  1985        PMID: 4045963      PMCID: PMC1049458          DOI: 10.1136/jmg.22.4.314

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  4 in total

1.  Small structural changes of chromosome 8. Two cases with evidence for deletion.

Authors:  C Beighle; L E Karp; J W Hanson; J G Hall; H Hoehn
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

2.  [Tricho-rhino-phalangeal syndrome].

Authors:  A Giedion
Journal:  Helv Paediatr Acta       Date:  1966-11

3.  Langer-Giedion syndrome, in a child with complex structural aberration of chromosome 8.

Authors:  D V Zaletajev; G S Marincheva
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Presumptive long arm deletion of chromosome 8: a new syndrome?

Authors:  K Taysi; M J Noetzel; A W Strauss
Journal:  Hum Genet       Date:  1979-09-02       Impact factor: 4.132

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.