| Literature DB >> 15456590 |
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.Entities:
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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