Title of article
Syndromic Congenital Chylothorax – a 7q21.13q31.31 Duplication
Author/Authors
Costa ، Raquel Monteiro Pediatric Department - Centro Hospitalar Tondela-Viseu , Martins ، Ana Isabel Pediatrics Hospital - Centro Hospitalar e Universitário de Coimbra , Sá ، Joaquim Genetic Department - Centro Hospitalar e Universitário de Coimbra , Silva ، Ana Rodrigues Neonatology Department - Centro Hospitalar e Universitário de Coimbra , Henriques ، Raquel Neonatology Department - Centro Hospitalar e Universitário de Coimbra
From page
15495
To page
15498
Abstract
Congenital chylothorax is a rare cause of respiratory distress in the newborns. It has a high mortality rate and its prognosis depends on the time of the diagnosis, etiology and therapy. The chromosomal gain, duplication of 28 Mb, including more than 200 genes, in the long arm of chromosome 7 (seq [GRCh37] 7q21.13q31.31, chr7:g.89783721_117877082dup) is very rare and is established as the likely etiology in this clinical case. Phenotypic reports of chromosomal imbalances are an important source for genetic counseling.
Keywords
Chromosomal gain , Congenital chylothorax , Genetic syndrome
Journal title
International Journal of Pediatrics
Journal title
International Journal of Pediatrics
Record number
2709537
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