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Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review

Abnormalities in the X-linked FMR1 gene are associated with a constellation of disorders, which have broad and profound implications for the person first diagnosed, and extended family members of all ages. The rare and pleiotropic nature of the associated disorders, both common and not, place great...

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Autores principales: Fink, Dorothy A., Nelson, Lawrence M., Pyeritz, Reed, Johnson, Josh, Sherman, Stephanie L., Cohen, Yoram, Elizur, Shai E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278244/
https://www.ncbi.nlm.nih.gov/pubmed/30542367
http://dx.doi.org/10.3389/fgene.2018.00529
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author Fink, Dorothy A.
Nelson, Lawrence M.
Pyeritz, Reed
Johnson, Josh
Sherman, Stephanie L.
Cohen, Yoram
Elizur, Shai E.
author_facet Fink, Dorothy A.
Nelson, Lawrence M.
Pyeritz, Reed
Johnson, Josh
Sherman, Stephanie L.
Cohen, Yoram
Elizur, Shai E.
author_sort Fink, Dorothy A.
collection PubMed
description Abnormalities in the X-linked FMR1 gene are associated with a constellation of disorders, which have broad and profound implications for the person first diagnosed, and extended family members of all ages. The rare and pleiotropic nature of the associated disorders, both common and not, place great burdens on (1) the affected families, (2) their care providers and clinicians, and (3) investigators striving to conduct research on the conditions. Fragile X syndrome, occurring more severely in males, is the leading genetic cause of intellectual disability. Fragile X associated tremor and ataxia syndrome (FXTAS) is a neurodegenerative disorder seen more often in older men. Fragile X associated primary ovarian insufficiency (FXPOI) is a chronic disorder characterized by oligo/amenorrhea and hypergonadotropic hypogonadism before age 40 years. There may be significant morbidity due to: (1) depression and anxiety related to the loss of reproductive hormones and infertility; (2) reduced bone mineral density; and (3) increased risk of cardiovascular disease related to estrogen deficiency. Here we report the case of a young woman who never established regular menses and yet experienced a 5-year diagnostic odyssey before establishing a diagnosis of FXPOI despite a known family history of fragile X syndrome and early menopause. Also, despite having clearly documented FXPOI the woman conceived spontaneously and delivered two healthy children. We review the pathophysiology and management of FXPOI. As a rare disease, the diagnosis of FXPOI presents special challenges. Connecting patients and community health providers with investigators who have the requisite knowledge and expertise about the FMR1 gene and FXPOI would facilitate both patient care and research. There is a need for an international natural history study on FXPOI. The effort should be coordinated by a global virtual center, which takes full advantage of mobile device communication systems.
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spelling pubmed-62782442018-12-12 Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review Fink, Dorothy A. Nelson, Lawrence M. Pyeritz, Reed Johnson, Josh Sherman, Stephanie L. Cohen, Yoram Elizur, Shai E. Front Genet Genetics Abnormalities in the X-linked FMR1 gene are associated with a constellation of disorders, which have broad and profound implications for the person first diagnosed, and extended family members of all ages. The rare and pleiotropic nature of the associated disorders, both common and not, place great burdens on (1) the affected families, (2) their care providers and clinicians, and (3) investigators striving to conduct research on the conditions. Fragile X syndrome, occurring more severely in males, is the leading genetic cause of intellectual disability. Fragile X associated tremor and ataxia syndrome (FXTAS) is a neurodegenerative disorder seen more often in older men. Fragile X associated primary ovarian insufficiency (FXPOI) is a chronic disorder characterized by oligo/amenorrhea and hypergonadotropic hypogonadism before age 40 years. There may be significant morbidity due to: (1) depression and anxiety related to the loss of reproductive hormones and infertility; (2) reduced bone mineral density; and (3) increased risk of cardiovascular disease related to estrogen deficiency. Here we report the case of a young woman who never established regular menses and yet experienced a 5-year diagnostic odyssey before establishing a diagnosis of FXPOI despite a known family history of fragile X syndrome and early menopause. Also, despite having clearly documented FXPOI the woman conceived spontaneously and delivered two healthy children. We review the pathophysiology and management of FXPOI. As a rare disease, the diagnosis of FXPOI presents special challenges. Connecting patients and community health providers with investigators who have the requisite knowledge and expertise about the FMR1 gene and FXPOI would facilitate both patient care and research. There is a need for an international natural history study on FXPOI. The effort should be coordinated by a global virtual center, which takes full advantage of mobile device communication systems. Frontiers Media S.A. 2018-11-27 /pmc/articles/PMC6278244/ /pubmed/30542367 http://dx.doi.org/10.3389/fgene.2018.00529 Text en Copyright © 2018 Fink, Nelson, Pyeritz, Johnson, Sherman, Cohen and Elizur. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Fink, Dorothy A.
Nelson, Lawrence M.
Pyeritz, Reed
Johnson, Josh
Sherman, Stephanie L.
Cohen, Yoram
Elizur, Shai E.
Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review
title Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review
title_full Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review
title_fullStr Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review
title_full_unstemmed Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review
title_short Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review
title_sort fragile x associated primary ovarian insufficiency (fxpoi): case report and literature review
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278244/
https://www.ncbi.nlm.nih.gov/pubmed/30542367
http://dx.doi.org/10.3389/fgene.2018.00529
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