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Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report

Primary hypothyroidism in the juvenile population generally leads to retardation of linear growth and delay or even arrest of puberty. However, in rare conditions, children with long-standing hypothyroidism present with signs of Van Wyk-Grumbach's syndrome (VWGS) which include juvenile hypothyr...

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Autores principales: Omran, Ahmed, Peng, Jing, Shrestha, Biswas, Ashhab, Muhammad Usman, Yin, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485864/
https://www.ncbi.nlm.nih.gov/pubmed/23133775
http://dx.doi.org/10.1155/2012/352751
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author Omran, Ahmed
Peng, Jing
Shrestha, Biswas
Ashhab, Muhammad Usman
Yin, Fei
author_facet Omran, Ahmed
Peng, Jing
Shrestha, Biswas
Ashhab, Muhammad Usman
Yin, Fei
author_sort Omran, Ahmed
collection PubMed
description Primary hypothyroidism in the juvenile population generally leads to retardation of linear growth and delay or even arrest of puberty. However, in rare conditions, children with long-standing hypothyroidism present with signs of Van Wyk-Grumbach's syndrome (VWGS) which include juvenile hypothyroidism, delayed bone age, and pseudoprecocious puberty. We report a rare case of prepubertal male child from Asian origin, presented with long-standing untreated hypothyroidism complicated with VWGS and other complications including obesity, short stature, hepatomegaly, asymptomatic mild pericardial effusion, and pituitary hyperplasia.
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spelling pubmed-34858642012-11-06 Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report Omran, Ahmed Peng, Jing Shrestha, Biswas Ashhab, Muhammad Usman Yin, Fei Case Rep Pediatr Case Report Primary hypothyroidism in the juvenile population generally leads to retardation of linear growth and delay or even arrest of puberty. However, in rare conditions, children with long-standing hypothyroidism present with signs of Van Wyk-Grumbach's syndrome (VWGS) which include juvenile hypothyroidism, delayed bone age, and pseudoprecocious puberty. We report a rare case of prepubertal male child from Asian origin, presented with long-standing untreated hypothyroidism complicated with VWGS and other complications including obesity, short stature, hepatomegaly, asymptomatic mild pericardial effusion, and pituitary hyperplasia. Hindawi Publishing Corporation 2012 2012-10-23 /pmc/articles/PMC3485864/ /pubmed/23133775 http://dx.doi.org/10.1155/2012/352751 Text en Copyright © 2012 Ahmed Omran et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under 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
Omran, Ahmed
Peng, Jing
Shrestha, Biswas
Ashhab, Muhammad Usman
Yin, Fei
Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report
title Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report
title_full Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report
title_fullStr Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report
title_full_unstemmed Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report
title_short Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report
title_sort male child with van wyk-grumbach's syndrome and other complications of long-standing primary hypothyroidism: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485864/
https://www.ncbi.nlm.nih.gov/pubmed/23133775
http://dx.doi.org/10.1155/2012/352751
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