| Registro completo |
| Provedor de dados: |
JBAG
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| País: |
Argentina
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| Título: |
Clinical and cytogenetic characterization of a patient with tetrasomy 18p
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| Autores: |
Vazquez Cantú,D.L
Gutiérrez García,V.M
Cruz-Camino,H
Lara Díaz,V.J
Garza García,K
Garduño Zarazúa,L.M
Meléndez Hernández,R
Paz Martínez,A
Mayén Molina,D.G
Cantú-Reyna,C
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| Data: |
2018-06-01
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| Ano: |
2018
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| Palavras-chave: |
Tetrasomy 18p
Chromosome 18
Isochromosome
Cytogenetic analysis
Case report
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| Resumo: |
The 18p tetrasomy is a structural chromosomal abnormality with the presence of an extra isochromosome 18p, caused by a nondisjunction failure during maternal meiosis II. This additional i(18p) occurs in 1 of 180,000 live-born children worldwide, affecting males and females equally. It is characterized by craniofacial dysmorphisms; ears, nose and throat (ENT) abnormalities; musculoskeletal alterations; and global development delay. We aim to present the clinical and cytogenetic findings of a 3-year-10-month-old Latin American male with i(18p), to support the gene dosage effects, comparing his features with the ones reported in literature. This patient was product of the second pregnancy of a 39-year-old woman and the first son of a 49-year-old man. His main clinical features were microcephaly, facial dysmorphism, generalized hypotonia, and developmental delay. A blood sample of the patient was required to perform a GTG-banded karyotype and a fluorescence in situ hybridization (FISH) for chromosome 18 short arm. In addition, an SNP microarray analysis was carried out to detect genomic imbalances. Cytogenetic analysis revealed the presence of a metacentric supernumerary marker chromosome. The FISH study confirmed the origin of the marker chromosome by showing two signals for the 18p subtelomere and an intermediate signal for the 18 centromere. The microarray analysis showed a copy number gain of 18,385 Mb within the 18p.Tetrasomy tends to be a result of de novo events. The presence of the patient’s isochromosome could be explained by advanced maternal age as it is known that this factor has high influence in isochromosome formation. Despite that there were no genes associated with the i(18p)’s clinical manifestations, these features are negatively correlated with dosage effects of the entire short arm. Physical and language therapy was recommended to the patient; the family received medical orientation, and awareness in family planning was raised.
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| Tipo: |
Info:eu-repo/semantics/article
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| Idioma: |
Inglês
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| Identificador: |
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S1852-62332018000100002
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| Editor: |
Sociedad Argentina de Genética
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| Formato: |
text/html
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| Fonte: |
BAG. Journal of basic and applied genetics v.29 n.1 2018
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| Direitos: |
info:eu-repo/semantics/openAccess
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