Abstract
Polycystic ovarian syndrome (PCOS) is a heterogenous disorder associated with clinical, endocrine and ultrasonographic features that can also be encountered in a number of other diseases. It has traditionally been suggested that prolactin excess, enzymatic steroidogenic abnormalities and thyroid disorders need to be excluded before a diagnosis of PCOS is made. However, there is paucity of data regarding the prevalence of PCOS phenotype in some of these disorders, whereas other endocrine diseases that exhibit PCOS-like features may elude diagnosis and proper management if not considered. This article reviews the data of currently included entities that exhibit a PCOS phenotype and those that potentially need to be looked for, and attempts to identify specific features that distinguish them from idiopathic PCOS.
| Original language | English |
|---|---|
| Pages (from-to) | 1-6 |
| Number of pages | 6 |
| Journal | Clinical Endocrinology |
| Volume | 86 |
| Issue number | 1 |
| Early online date | 11 Oct 2016 |
| DOIs | |
| Publication status | Published - 1 Jan 2017 |
Bibliographical note
This is the peer reviewed version of the following article: Kyritsi, E. M., Dimitriadis, G. K., Kyrou, I., Kaltsas, G., & Randeva, H. S. (2017). PCOS remains a diagnosis of exclusion: a concise review of key endocrinopathies to exclude. Clinical Endocrinology, 86 (1) 1-6, which has been published in final form at http://dx.doi.org/10.1111/cen.13245. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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