| Texto completo | |
| Autor(es): |
Bragagnolo, Silvia
;
Colovati, Mileny E. S.
;
Guilherme, Roberta S.
;
Dantas, Anelisa G.
;
de Souza, Malu Zamariolli
;
de Soares, Maria F.
;
Melaragno, Maria I.
;
Perez, Ana B.
Número total de Autores: 8
|
| Tipo de documento: | Artigo Científico |
| Fonte: | Cytogenetic and Genome Research; v. 150, n. 1, p. 17-22, 2016. |
| Citações Web of Science: | 2 |
| Resumo | |
Wolf-Hirschhorn syndrome (WHS) is a contiguous gene and multiple malformation syndrome that results from a deletion in the 4p16.3 region. We describe here a 6-month-old girl that presented with WHS features but also displayed unusual findings, such as epibulbar dermoid in the left eye, ear tags, and left microtia. Although on G-banding her karyotype appeared to be normal, chromosomal microarray analysis revealed an similar to 13-Mb 4p16.3p15.33 deletion and an similar to 9-Mb Xp22.33p22.31 duplication, resulting from a balanced maternal t(X; 4)(p22.31; p15.33) translocation. The patient presented with functional Xp disomy due to an unbalanced X-autosome translocation, a rare cytogenetic finding in females with unbalanced rearrangements. Sequencing of both chromosome breakpoints detected no gene disruption. To the best of our knowledge, this is the first patient described in the literature with WHS and epibulbar dermoid, a typical characteristic of the oculoauriculovertebral spectrum (OAVS). Our data suggest that possible candidate genes for OAVS may have been deleted along with the WHS critical region. (C) 2016 S. Karger AG, Basel (AU) | |
| Processo FAPESP: | 13/04623-2 - Síndrome de Goldenhar e espectro óculo-aurículo-vertebral (GS/OAVS): estudo clínico, citogenômico e molecular |
| Beneficiário: | Ana Beatriz Alvarez Perez |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |