Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp
We report a male patient with three copy-number variations (CNVs) and unique phenotype. He carried ~11.2 Mb terminal duplication on 4q, ~13.4 Mb terminal deletion on 7q and ~1.7 Mb interstitial duplication on Xp22.31, which were identified by array-based comparative genomic hybridization. He manifes...
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Nature Publishing Group
2015
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pubmed-47855762016-04-14 Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp Okuno, Misako Ogata, Tsutomu Nakabayashi, Kazuhiko Urakami, Tatsuhiko Fukami, Maki Nagasaki, Keisuke Data Report We report a male patient with three copy-number variations (CNVs) and unique phenotype. He carried ~11.2 Mb terminal duplication on 4q, ~13.4 Mb terminal deletion on 7q and ~1.7 Mb interstitial duplication on Xp22.31, which were identified by array-based comparative genomic hybridization. He manifested mental retardation, mild brain anomalies and skeletal deformities ascribable to these CNVs, together with central precocious puberty and mild adrenocorticotropic hormone overproduction of unknown etiologies. Nature Publishing Group 2015-07-02 /pmc/articles/PMC4785576/ /pubmed/27081533 http://dx.doi.org/10.1038/hgv.2015.20 Text en Copyright © 2015 The Japan Society of Human Genetics http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
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Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Okuno, Misako Ogata, Tsutomu Nakabayashi, Kazuhiko Urakami, Tatsuhiko Fukami, Maki Nagasaki, Keisuke |
spellingShingle |
Okuno, Misako Ogata, Tsutomu Nakabayashi, Kazuhiko Urakami, Tatsuhiko Fukami, Maki Nagasaki, Keisuke Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp |
author_facet |
Okuno, Misako Ogata, Tsutomu Nakabayashi, Kazuhiko Urakami, Tatsuhiko Fukami, Maki Nagasaki, Keisuke |
author_sort |
Okuno, Misako |
title |
Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp |
title_short |
Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp |
title_full |
Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp |
title_fullStr |
Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp |
title_full_unstemmed |
Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp |
title_sort |
endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and xp |
description |
We report a male patient with three copy-number variations (CNVs) and unique phenotype. He carried ~11.2 Mb terminal duplication on 4q, ~13.4 Mb terminal deletion on 7q and ~1.7 Mb interstitial duplication on Xp22.31, which were identified by array-based comparative genomic hybridization. He manifested mental retardation, mild brain anomalies and skeletal deformities ascribable to these CNVs, together with central precocious puberty and mild adrenocorticotropic hormone overproduction of unknown etiologies. |
publisher |
Nature Publishing Group |
publishDate |
2015 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785576/ |
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1613549947894890496 |