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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell Lines

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Author(s):
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Gasparini, Yanca [1] ; Montenegro, Marilia M. [1] ; Novo-Filho, Gil M. [1] ; Ceroni, Jose R. M. [2] ; Honjo, Rachel S. [2] ; Zanardo, Evelin A. [1] ; Dias, Alexandre T. [1] ; Nascimento, Amom M. [1] ; Costa, Thais V. M. M. [1] ; Madia, Fabricia A. [1] ; Chehimi, Samar N. [1] ; Damasceno, Jullian G. [1] ; Kim, Chong A. [2] ; Kulikowski, Leslie D. [1]
Total Authors: 14
Affiliation:
[1] Univ Sao Paulo, Hosp Clin HCFMUSP, Inst Crianca, Lab Citogen, Dept Patol, Fac Med, Sao Paulo - Brazil
[2] Univ Sao Paulo, Hosp Clin HCFMUSP, Inst Crianca, Unidade Genet, Dept Pediat, Fac Med, Sao Paulo - Brazil
Total Affiliations: 2
Document type: Journal article
Source: Cytogenetic and Genome Research; v. 157, n. 3, p. 153-157, 2019.
Web of Science Citations: 1
Abstract

Mosaic trisomy 12 is a rare anomaly, and only 9 cases of live births with this condition have been reported in the literature. The clinical phenotype is variable, including neuropsychomotor developmental delay, congenital heart disease, microcephaly, cutaneous spots, facial asymmetry, prominent ears, hypotonia, retinopathy, and sensorineural hearing loss. A 2-year-old female presented with neuropsychomotor developmental delay, prominent forehead, dolichocephaly, patchy skin pigmentation, and unexpected over-growth at birth. Cytogenetic analysis of her peripheral blood showed normal results, suggesting the presence of a chromosomal alteration in other tissues. Further studies using G-banding and FISH performed on fibroblasts from both hyper-and hypopigmented regions identified a 47, XX,+12/46, XX karyo-type. To the best of our knowledge, no patients with mosaic trisomy 12 associated with overgrowth have been reported to date. Congenital overgrowth and neonatal overgrowth have been frequently linked to Pallister-Killian syndrome (PKS; OMIM 601803). This case suggests the possibility of an association of genes present in the 12p region with fetal overgrowth, considering that chromosomal duplications could lead to an increase in the production of aberrant transcripts and disturbing gene dosage effects. This case highlights the importance of cytogenetic analysis in different tissues to provide relevant information to the specific genotype/phenotype correlation. (c) 2019 S. Karger AG, Basel. (AU)

FAPESP's process: 16/19360-5 - Chromosome and subtelomeric study by the G-banding and MLPA technique in pigmentation abnormalities from patients with syndromes associated with malformation
Grantee:Yanca Gasparini de Oliveira
Support type: Scholarships in Brazil - Scientific Initiation
FAPESP's process: 16/09452-0 - Mapping of DNA break points and investigation of the mechanisms associated with genomic rearrangements using next generation sequencing.
Grantee:Leslie Domenici Kulikowski
Support type: Regular Research Grants