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Severe Short Stature: an unusual finding in lipoid proteinosis

Lipoid proteinosis (LP) is a rare disorder and it can affect every organ in the body. The clinical manifestations of LP may vary considerably between affected individuals. Short stature is reported in patients with LP however the underlying etiology is not clear. Short stature may be due to endocrin...

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Autores principales: Poyrazoğlu, Şükran, Günöz, Hülya, Darendeliler, Feyza
Formato: Texto
Lenguaje:English
Publicado: Galenos Publishing 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005640/
https://www.ncbi.nlm.nih.gov/pubmed/21318070
http://dx.doi.org/10.4008/jcrpe.v1i2.31
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author Poyrazoğlu, Şükran
Günöz, Hülya
Darendeliler, Feyza
author_facet Poyrazoğlu, Şükran
Günöz, Hülya
Darendeliler, Feyza
author_sort Poyrazoğlu, Şükran
collection PubMed
description Lipoid proteinosis (LP) is a rare disorder and it can affect every organ in the body. The clinical manifestations of LP may vary considerably between affected individuals. Short stature is reported in patients with LP however the underlying etiology is not clear. Short stature may be due to endocrine dysfunction caused by deposition of hyaline−like material in endocrine glands. We investigated a 13 year old patient with LP (507 delT mutation) who had severe short stature. He had hoarseness since the age of one year, followed by characteristic skin lesions for LP and short stature. There was no pathology with respect to endocrinological investigations in our patient including growth hormone−IGF axis. Our results show that short stature in LP can not be explained by endocrinological abnormalities. Short stature may be an intrinsic component of the syndrome. Conflict of interest:None declared.
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spelling pubmed-30056402011-01-27 Severe Short Stature: an unusual finding in lipoid proteinosis Poyrazoğlu, Şükran Günöz, Hülya Darendeliler, Feyza J Clin Res Pediatr Endocrinol Case Reports Lipoid proteinosis (LP) is a rare disorder and it can affect every organ in the body. The clinical manifestations of LP may vary considerably between affected individuals. Short stature is reported in patients with LP however the underlying etiology is not clear. Short stature may be due to endocrine dysfunction caused by deposition of hyaline−like material in endocrine glands. We investigated a 13 year old patient with LP (507 delT mutation) who had severe short stature. He had hoarseness since the age of one year, followed by characteristic skin lesions for LP and short stature. There was no pathology with respect to endocrinological investigations in our patient including growth hormone−IGF axis. Our results show that short stature in LP can not be explained by endocrinological abnormalities. Short stature may be an intrinsic component of the syndrome. Conflict of interest:None declared. Galenos Publishing 2008-12 2008-11-06 /pmc/articles/PMC3005640/ /pubmed/21318070 http://dx.doi.org/10.4008/jcrpe.v1i2.31 Text en © Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing. 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 Reports
Poyrazoğlu, Şükran
Günöz, Hülya
Darendeliler, Feyza
Severe Short Stature: an unusual finding in lipoid proteinosis
title Severe Short Stature: an unusual finding in lipoid proteinosis
title_full Severe Short Stature: an unusual finding in lipoid proteinosis
title_fullStr Severe Short Stature: an unusual finding in lipoid proteinosis
title_full_unstemmed Severe Short Stature: an unusual finding in lipoid proteinosis
title_short Severe Short Stature: an unusual finding in lipoid proteinosis
title_sort severe short stature: an unusual finding in lipoid proteinosis
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005640/
https://www.ncbi.nlm.nih.gov/pubmed/21318070
http://dx.doi.org/10.4008/jcrpe.v1i2.31
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