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45,X/46,X,psu idic(Y)(q11.2) in a phenotypically normal male with short stature: a case report
We report a case of 15-yr-old phenotypically normal male with short stature associated with the chromosomal abnormalities of 46,X,psu idic(Y)(q11.2)/45,X. At 3 yr of age, he underwent urethroplasty for scrotal hypospadias. At 15 yr of age, he was referred to our hospital due to short stature (–3.71...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society for Pediatric Endocrinology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534520/ https://www.ncbi.nlm.nih.gov/pubmed/33088019 http://dx.doi.org/10.1297/cpe.29.189 |
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author | Kawabe, Yasuhiro Yamaguchi, Mihoko Miyagaki, Satoshi Ota, Takeshi Morimoto, Hidechika Hattori, Atsushi Fukami, Maki Mori, Jun |
author_facet | Kawabe, Yasuhiro Yamaguchi, Mihoko Miyagaki, Satoshi Ota, Takeshi Morimoto, Hidechika Hattori, Atsushi Fukami, Maki Mori, Jun |
author_sort | Kawabe, Yasuhiro |
collection | PubMed |
description | We report a case of 15-yr-old phenotypically normal male with short stature associated with the chromosomal abnormalities of 46,X,psu idic(Y)(q11.2)/45,X. At 3 yr of age, he underwent urethroplasty for scrotal hypospadias. At 15 yr of age, he was referred to our hospital due to short stature (–3.71 SD). The results of blood examination were mostly normal. A radiological examination revealed his bone age was 15.7 yr (based on the TW2-RUS method). Chromosome analysis of peripheral lymphocytes revealed 46,X,psu idic(Y)(q11.2)[16]/45,X[14], and array comparative genomic hybridization (aCGH) showed a large deletion of Yq which was located distal to the Y chromosome growth-control gene (GCY) region. It is likely that these structural abnormalities in the Y chromosome were responsible for the short stature. This case might provide new insights regarding GCY and emphasizes the importance of chromosome analysis in not only females but also males with short stature, especially when associated with genital anomalies. |
format | Online Article Text |
id | pubmed-7534520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Japanese Society for Pediatric Endocrinology |
record_format | MEDLINE/PubMed |
spelling | pubmed-75345202020-10-20 45,X/46,X,psu idic(Y)(q11.2) in a phenotypically normal male with short stature: a case report Kawabe, Yasuhiro Yamaguchi, Mihoko Miyagaki, Satoshi Ota, Takeshi Morimoto, Hidechika Hattori, Atsushi Fukami, Maki Mori, Jun Clin Pediatr Endocrinol Case Report We report a case of 15-yr-old phenotypically normal male with short stature associated with the chromosomal abnormalities of 46,X,psu idic(Y)(q11.2)/45,X. At 3 yr of age, he underwent urethroplasty for scrotal hypospadias. At 15 yr of age, he was referred to our hospital due to short stature (–3.71 SD). The results of blood examination were mostly normal. A radiological examination revealed his bone age was 15.7 yr (based on the TW2-RUS method). Chromosome analysis of peripheral lymphocytes revealed 46,X,psu idic(Y)(q11.2)[16]/45,X[14], and array comparative genomic hybridization (aCGH) showed a large deletion of Yq which was located distal to the Y chromosome growth-control gene (GCY) region. It is likely that these structural abnormalities in the Y chromosome were responsible for the short stature. This case might provide new insights regarding GCY and emphasizes the importance of chromosome analysis in not only females but also males with short stature, especially when associated with genital anomalies. The Japanese Society for Pediatric Endocrinology 2020-10-03 2020 /pmc/articles/PMC7534520/ /pubmed/33088019 http://dx.doi.org/10.1297/cpe.29.189 Text en 2020©The Japanese Society for Pediatric Endocrinology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Kawabe, Yasuhiro Yamaguchi, Mihoko Miyagaki, Satoshi Ota, Takeshi Morimoto, Hidechika Hattori, Atsushi Fukami, Maki Mori, Jun 45,X/46,X,psu idic(Y)(q11.2) in a phenotypically normal male with short stature: a case report |
title | 45,X/46,X,psu idic(Y)(q11.2) in a phenotypically normal male with short
stature: a case report |
title_full | 45,X/46,X,psu idic(Y)(q11.2) in a phenotypically normal male with short
stature: a case report |
title_fullStr | 45,X/46,X,psu idic(Y)(q11.2) in a phenotypically normal male with short
stature: a case report |
title_full_unstemmed | 45,X/46,X,psu idic(Y)(q11.2) in a phenotypically normal male with short
stature: a case report |
title_short | 45,X/46,X,psu idic(Y)(q11.2) in a phenotypically normal male with short
stature: a case report |
title_sort | 45,x/46,x,psu idic(y)(q11.2) in a phenotypically normal male with short
stature: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534520/ https://www.ncbi.nlm.nih.gov/pubmed/33088019 http://dx.doi.org/10.1297/cpe.29.189 |
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