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Parsing Genetic and Autoimmune Etiology in Premature Ovarian Insufficiency

Premature ovarian insufficiency (POI) is a rare cause of primary amenorrhea in adolescents. For young women with uncertain etiology of POI, genetic and autoimmune testing may be recommended to assist in treatment and management decisions. This report presents a case of POI in a 16-year-old adolescen...

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Autores principales: Nauwynck, Elise, De Schepper, Jean, De Vos, Michel, Staels, Willem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690725/
https://www.ncbi.nlm.nih.gov/pubmed/38045866
http://dx.doi.org/10.1210/jcemcr/luad124
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author Nauwynck, Elise
De Schepper, Jean
De Vos, Michel
Staels, Willem
author_facet Nauwynck, Elise
De Schepper, Jean
De Vos, Michel
Staels, Willem
author_sort Nauwynck, Elise
collection PubMed
description Premature ovarian insufficiency (POI) is a rare cause of primary amenorrhea in adolescents. For young women with uncertain etiology of POI, genetic and autoimmune testing may be recommended to assist in treatment and management decisions. This report presents a case of POI in a 16-year-old adolescent with both poly-autoimmune disease and a heterozygous missense variant in the bone morphogenic factor 15 (BMP15) gene, both potentially involved in the pathogenesis of POI. Accurately distinguishing between autoimmune and genetic causes is crucial for effective treatment and counseling. In addition, given the significant psychological impact and the need for reproductive options counseling, a multidisciplinary approach that includes psychological support is highly recommended.
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spelling pubmed-106907252023-12-02 Parsing Genetic and Autoimmune Etiology in Premature Ovarian Insufficiency Nauwynck, Elise De Schepper, Jean De Vos, Michel Staels, Willem JCEM Case Rep Case Report Premature ovarian insufficiency (POI) is a rare cause of primary amenorrhea in adolescents. For young women with uncertain etiology of POI, genetic and autoimmune testing may be recommended to assist in treatment and management decisions. This report presents a case of POI in a 16-year-old adolescent with both poly-autoimmune disease and a heterozygous missense variant in the bone morphogenic factor 15 (BMP15) gene, both potentially involved in the pathogenesis of POI. Accurately distinguishing between autoimmune and genetic causes is crucial for effective treatment and counseling. In addition, given the significant psychological impact and the need for reproductive options counseling, a multidisciplinary approach that includes psychological support is highly recommended. Oxford University Press 2023-12-01 /pmc/articles/PMC10690725/ /pubmed/38045866 http://dx.doi.org/10.1210/jcemcr/luad124 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nauwynck, Elise
De Schepper, Jean
De Vos, Michel
Staels, Willem
Parsing Genetic and Autoimmune Etiology in Premature Ovarian Insufficiency
title Parsing Genetic and Autoimmune Etiology in Premature Ovarian Insufficiency
title_full Parsing Genetic and Autoimmune Etiology in Premature Ovarian Insufficiency
title_fullStr Parsing Genetic and Autoimmune Etiology in Premature Ovarian Insufficiency
title_full_unstemmed Parsing Genetic and Autoimmune Etiology in Premature Ovarian Insufficiency
title_short Parsing Genetic and Autoimmune Etiology in Premature Ovarian Insufficiency
title_sort parsing genetic and autoimmune etiology in premature ovarian insufficiency
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690725/
https://www.ncbi.nlm.nih.gov/pubmed/38045866
http://dx.doi.org/10.1210/jcemcr/luad124
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