Literature DB >> 6985014

Tetrasomy 9p: clinical aspects and enzymatic gene dosage expression.

D Garcia-Cruz, G Vaca, B Ibarra, J Sánchez-Corona, R Ocampo-Campos, S Peregrina, M Moller, H Rivera, F Rivas, A González-Angulo, J M Cantu.   

Abstract

A girl aged 13 years and 9 months with a phenotypic appearance of 9p trisomy was studied. Chromosome analysis of peripheral blood lymphocytes revealed a 9p tetrasomy [47,XX,+i(9p)] with no evidence of mosaicism. Biochemical studies corroborate the gene dosage effect for galactose-1-phosphate uridyltransferase. The roentgenological findings were quite similar to those of the 9p trisomy except for hypoplastic and angulated ribs, and malformed vertebral bodies, which are probably exclusive of the tetrasomic state.

Entities:  

Mesh:

Year:  1982        PMID: 6985014

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


  2 in total

1.  Partial tetrasomy 9 in an infant with clinical and radiological evidence of multiple joint dislocations.

Authors:  F Calvieri; C Tozzi; C Benincori; M V De Merulis; A Bellussi; M Genuardi; G Neri
Journal:  Eur J Pediatr       Date:  1988-08       Impact factor: 3.183

2.  Tetrasomy 9p confirmed by GALT.

Authors:  P Balestrazzi; G Croci; C Frassi; F Franchi; G Giovannelli
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.