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Familial HCG syndrome: A diagnostic challenge
• This is a rare inheritable condition which results in raised total HCG levels. • Common causes of raised HCG need to be excluded prior to considering this syndrome. • A diagnosis can prevent unnecessary surgical or oncological treatment.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458743/ https://www.ncbi.nlm.nih.gov/pubmed/26082938 http://dx.doi.org/10.1016/j.gynor.2014.05.005 |
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author | Tan, Alvin Van der Merwe, Anna-Marie Low, Xunjun Chrystal, Kathryn |
author_facet | Tan, Alvin Van der Merwe, Anna-Marie Low, Xunjun Chrystal, Kathryn |
author_sort | Tan, Alvin |
collection | PubMed |
description | • This is a rare inheritable condition which results in raised total HCG levels. • Common causes of raised HCG need to be excluded prior to considering this syndrome. • A diagnosis can prevent unnecessary surgical or oncological treatment. |
format | Online Article Text |
id | pubmed-4458743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-44587432015-06-16 Familial HCG syndrome: A diagnostic challenge Tan, Alvin Van der Merwe, Anna-Marie Low, Xunjun Chrystal, Kathryn Gynecol Oncol Rep Case Report • This is a rare inheritable condition which results in raised total HCG levels. • Common causes of raised HCG need to be excluded prior to considering this syndrome. • A diagnosis can prevent unnecessary surgical or oncological treatment. Elsevier 2014-06-01 /pmc/articles/PMC4458743/ /pubmed/26082938 http://dx.doi.org/10.1016/j.gynor.2014.05.005 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open access article under the CC BY-NC-SA license (http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Case Report Tan, Alvin Van der Merwe, Anna-Marie Low, Xunjun Chrystal, Kathryn Familial HCG syndrome: A diagnostic challenge |
title | Familial HCG syndrome: A diagnostic challenge |
title_full | Familial HCG syndrome: A diagnostic challenge |
title_fullStr | Familial HCG syndrome: A diagnostic challenge |
title_full_unstemmed | Familial HCG syndrome: A diagnostic challenge |
title_short | Familial HCG syndrome: A diagnostic challenge |
title_sort | familial hcg syndrome: a diagnostic challenge |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458743/ https://www.ncbi.nlm.nih.gov/pubmed/26082938 http://dx.doi.org/10.1016/j.gynor.2014.05.005 |
work_keys_str_mv | AT tanalvin familialhcgsyndromeadiagnosticchallenge AT vandermerweannamarie familialhcgsyndromeadiagnosticchallenge AT lowxunjun familialhcgsyndromeadiagnosticchallenge AT chrystalkathryn familialhcgsyndromeadiagnosticchallenge |