Literature DB >> 15456590

[Trisomy 9p. Report of two new cases].

M San Román Muñoz1, J L Herranz Fernández, A Tejerina Puente, R Arteaga Manjón-Cabeza, F López Grondona.   

Abstract

Trisomy 9p is a chromosome abnormality caused by duplication of the short arm of chromosome 9. Clinically it is characterized by psychomotor retardation, malformations that can affect various organs and sometimes epilepsy. Trisomy 9p may be the fourth most common autosomal trisomy, after trisomies 21, 13 and 18. Two new cases of trisomy 9p are described. Previous cases reported in Spain, associated clinical features, and the diagnostic and therapeutic approach to these patients are revised.

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Year:  2004        PMID: 15456590     DOI: 10.1016/s1695-4033(04)78398-8

Source DB:  PubMed          Journal:  An Pediatr (Barc)        ISSN: 1695-4033            Impact factor:   1.500


  2 in total

1.  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.  Partial trisomy 9: prenatal diagnosis and recurrence within same family.

Authors:  Jana López-Félix; Leticia Flores-Gallegos; Luz Garduño-Zarazúa; Teresa Leis-Márquez; Luz Juárez-García; Ricardo Meléndez-Hernández; Ernesto Castelazo-Morales; Dora Mayén-Molina
Journal:  Clin Case Rep       Date:  2017-05-10
  2 in total

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