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Non-Classical Congenital Adrenal Hyperplasia in Childhood
Congenital adrenal hyperplasia (CAH) is classified as classical CAH and non-classical CAH (NCCAH). In the classical type, the most severe form comprises both salt-wasting and simple virilizing forms. In the non-classical form, diagnosis can be more confusing because the patient may remain asymptomat...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363159/ https://www.ncbi.nlm.nih.gov/pubmed/27354284 http://dx.doi.org/10.4274/jcrpe.3378 |
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author | Kurtoğlu, Selim Hatipoğlu, Nihal |
author_facet | Kurtoğlu, Selim Hatipoğlu, Nihal |
author_sort | Kurtoğlu, Selim |
collection | PubMed |
description | Congenital adrenal hyperplasia (CAH) is classified as classical CAH and non-classical CAH (NCCAH). In the classical type, the most severe form comprises both salt-wasting and simple virilizing forms. In the non-classical form, diagnosis can be more confusing because the patient may remain asymptomatic or the condition may be associated with signs of androgen excess in the postnatal period or in the later stages of life. This review paper will include information on clinical findings, symptoms, diagnostic approaches, and treatment modules of NCCAH. |
format | Online Article Text |
id | pubmed-5363159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Galenos Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-53631592017-04-04 Non-Classical Congenital Adrenal Hyperplasia in Childhood Kurtoğlu, Selim Hatipoğlu, Nihal J Clin Res Pediatr Endocrinol Review Congenital adrenal hyperplasia (CAH) is classified as classical CAH and non-classical CAH (NCCAH). In the classical type, the most severe form comprises both salt-wasting and simple virilizing forms. In the non-classical form, diagnosis can be more confusing because the patient may remain asymptomatic or the condition may be associated with signs of androgen excess in the postnatal period or in the later stages of life. This review paper will include information on clinical findings, symptoms, diagnostic approaches, and treatment modules of NCCAH. Galenos Publishing 2017-03 2017-03-01 /pmc/articles/PMC5363159/ /pubmed/27354284 http://dx.doi.org/10.4274/jcrpe.3378 Text en © 2017 by Turkish Pediatric Endocrinology and Diabetes Society http://creativecommons.org/licenses/by/2.5/ The Journal of Clinical Research in Pediatric Endocrinology published by Galenos Publishing House. |
spellingShingle | Review Kurtoğlu, Selim Hatipoğlu, Nihal Non-Classical Congenital Adrenal Hyperplasia in Childhood |
title | Non-Classical Congenital Adrenal Hyperplasia in Childhood |
title_full | Non-Classical Congenital Adrenal Hyperplasia in Childhood |
title_fullStr | Non-Classical Congenital Adrenal Hyperplasia in Childhood |
title_full_unstemmed | Non-Classical Congenital Adrenal Hyperplasia in Childhood |
title_short | Non-Classical Congenital Adrenal Hyperplasia in Childhood |
title_sort | non-classical congenital adrenal hyperplasia in childhood |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363159/ https://www.ncbi.nlm.nih.gov/pubmed/27354284 http://dx.doi.org/10.4274/jcrpe.3378 |
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