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XYY syndrome: a 13-year-old boy with tall stature

When evaluating the underlying causes of tall stature, it is important to differentiate pathologic tall stature from familial tall stature. Various pathologic conditions leading to adult tall stature include excess growth hormone secretion, Marfan syndrome, androgen or estrogen deficiency, testicula...

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Detalles Bibliográficos
Autores principales: Jo, Won Ha, Jung, Mo Kyung, Kim, Ki Eun, Chae, Hyun Wook, Kim, Duk Hee, Kwon, Ah Reum, Kim, Ho-Seong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623347/
https://www.ncbi.nlm.nih.gov/pubmed/26512355
http://dx.doi.org/10.6065/apem.2015.20.3.170
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author Jo, Won Ha
Jung, Mo Kyung
Kim, Ki Eun
Chae, Hyun Wook
Kim, Duk Hee
Kwon, Ah Reum
Kim, Ho-Seong
author_facet Jo, Won Ha
Jung, Mo Kyung
Kim, Ki Eun
Chae, Hyun Wook
Kim, Duk Hee
Kwon, Ah Reum
Kim, Ho-Seong
author_sort Jo, Won Ha
collection PubMed
description When evaluating the underlying causes of tall stature, it is important to differentiate pathologic tall stature from familial tall stature. Various pathologic conditions leading to adult tall stature include excess growth hormone secretion, Marfan syndrome, androgen or estrogen deficiency, testicular feminization, and sex chromosome anomaly, such as Klinefelter syndrome and XYY syndrome. Men with 47,XYY syndrome can exhibit multiple phenotypes. A 13-year-old boy visited the hospital for evaluation of tall stature. The boy had no other physical abnormalities except tall stature. All biochemical and imaging studies were within the normal ranges. He was diagnosed with XYY syndrome in this chromosome study. When evaluating men with tall stature, XYY syndrome should be ruled out.
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spelling pubmed-46233472015-10-28 XYY syndrome: a 13-year-old boy with tall stature Jo, Won Ha Jung, Mo Kyung Kim, Ki Eun Chae, Hyun Wook Kim, Duk Hee Kwon, Ah Reum Kim, Ho-Seong Ann Pediatr Endocrinol Metab Case Report When evaluating the underlying causes of tall stature, it is important to differentiate pathologic tall stature from familial tall stature. Various pathologic conditions leading to adult tall stature include excess growth hormone secretion, Marfan syndrome, androgen or estrogen deficiency, testicular feminization, and sex chromosome anomaly, such as Klinefelter syndrome and XYY syndrome. Men with 47,XYY syndrome can exhibit multiple phenotypes. A 13-year-old boy visited the hospital for evaluation of tall stature. The boy had no other physical abnormalities except tall stature. All biochemical and imaging studies were within the normal ranges. He was diagnosed with XYY syndrome in this chromosome study. When evaluating men with tall stature, XYY syndrome should be ruled out. The Korean Society of Pediatric Endocrinology 2015-09 2015-09-30 /pmc/articles/PMC4623347/ /pubmed/26512355 http://dx.doi.org/10.6065/apem.2015.20.3.170 Text en © 2015 Annals of Pediatric Endocrinology & Metabolism http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jo, Won Ha
Jung, Mo Kyung
Kim, Ki Eun
Chae, Hyun Wook
Kim, Duk Hee
Kwon, Ah Reum
Kim, Ho-Seong
XYY syndrome: a 13-year-old boy with tall stature
title XYY syndrome: a 13-year-old boy with tall stature
title_full XYY syndrome: a 13-year-old boy with tall stature
title_fullStr XYY syndrome: a 13-year-old boy with tall stature
title_full_unstemmed XYY syndrome: a 13-year-old boy with tall stature
title_short XYY syndrome: a 13-year-old boy with tall stature
title_sort xyy syndrome: a 13-year-old boy with tall stature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623347/
https://www.ncbi.nlm.nih.gov/pubmed/26512355
http://dx.doi.org/10.6065/apem.2015.20.3.170
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