Artículos de revistas
A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion
Registro en:
Gene. Elsevier Science Bv, v. 523, n. 2, n. 192, n. 194, 2013.
0378-1119
WOS:000320424400013
10.1016/j.gene.2013.03.115
Autor
Sgardioli, IC
Simioni, M
Viguetti-Campos, NL
Prota, JR
Gil-da-Silva-Lopes, VL
Institución
Resumen
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Chromosome 14 is often involved in chromosome rearrangements, although pericentric inversions are rare. Here we report a mother carrying a pericentric inversion of chromosome 14, and her daughter with recombinant chromosome characterized by a partial distal 14q trisomy. Principal clinical findings of the child include facial anomalies, microcephaly, developmental delay, hypotonia and cardiac malformation. Her final karyotype was 46,XX,rec(14)dup(14q)inv(14)(p12q31)mat[20], arr 14q31.3qter(85,427,839-106,356,482) x3. This report brings new data about clinical features of partial 14q trisomy and molecular analysis enables the visualization of genes involved in the segment duplicated. (C) 2013 Elsevier B.V. All rights reserved. 523 2 192 194 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) FAPESP [2008/10596-0] CNPq [CNPq 304455/2012-1]