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Chromosome Duplication (14q) and The Genotype Phenotype Correlation

The rearrangement of chromosome 14 is a rare cytogenetic finding. Changes in the number or structure of chromosome 14 can have a variety of effects, such as delayed growth and development, and distinctive facial features. The human chromosome 14 plays an important role in imprinting events importune...

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Autores principales: Sadr-Nabavi, Ariane, Saeidi, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973161/
https://www.ncbi.nlm.nih.gov/pubmed/24696773
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author Sadr-Nabavi, Ariane
Saeidi, Morteza
author_facet Sadr-Nabavi, Ariane
Saeidi, Morteza
author_sort Sadr-Nabavi, Ariane
collection PubMed
description The rearrangement of chromosome 14 is a rare cytogenetic finding. Changes in the number or structure of chromosome 14 can have a variety of effects, such as delayed growth and development, and distinctive facial features. The human chromosome 14 plays an important role in imprinting events importunes of a structural rearrangement is specifically when a phenotype is caused by imprinting, whereby the interpretation of genotype-phenotype correlation becomes extremely difficult. In this study, we examined a 3 year-old mentally impaired girl with unusual facial features. G-banding showed terminal duplication of chromosome 14 in the karyotype of the patient. In this particular case, we explained a phenotype genotype correlation in a patient with a dup (14) rearrangement, thus emphasizing the importance of prenatal diagnosis for pregnancies with an abnormal nuchal translucency.
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spelling pubmed-39731612014-04-02 Chromosome Duplication (14q) and The Genotype Phenotype Correlation Sadr-Nabavi, Ariane Saeidi, Morteza Int J Fertil Steril Case Report The rearrangement of chromosome 14 is a rare cytogenetic finding. Changes in the number or structure of chromosome 14 can have a variety of effects, such as delayed growth and development, and distinctive facial features. The human chromosome 14 plays an important role in imprinting events importunes of a structural rearrangement is specifically when a phenotype is caused by imprinting, whereby the interpretation of genotype-phenotype correlation becomes extremely difficult. In this study, we examined a 3 year-old mentally impaired girl with unusual facial features. G-banding showed terminal duplication of chromosome 14 in the karyotype of the patient. In this particular case, we explained a phenotype genotype correlation in a patient with a dup (14) rearrangement, thus emphasizing the importance of prenatal diagnosis for pregnancies with an abnormal nuchal translucency. Royan Institute 2014 2014-03-09 /pmc/articles/PMC3973161/ /pubmed/24696773 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sadr-Nabavi, Ariane
Saeidi, Morteza
Chromosome Duplication (14q) and The Genotype Phenotype Correlation
title Chromosome Duplication (14q) and The Genotype Phenotype Correlation
title_full Chromosome Duplication (14q) and The Genotype Phenotype Correlation
title_fullStr Chromosome Duplication (14q) and The Genotype Phenotype Correlation
title_full_unstemmed Chromosome Duplication (14q) and The Genotype Phenotype Correlation
title_short Chromosome Duplication (14q) and The Genotype Phenotype Correlation
title_sort chromosome duplication (14q) and the genotype phenotype correlation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973161/
https://www.ncbi.nlm.nih.gov/pubmed/24696773
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