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Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report
INTRODUCTION: Premature ovarian failure is defined as the cessation of ovarian activity before the age of 40 years. It is biochemically characterized by low levels of gonadal hormones (estrogens and inhibins) and high levels of gonadotropins (luteinizing hormone and follicle-stimulating hormone). CA...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520733/ https://www.ncbi.nlm.nih.gov/pubmed/23107510 http://dx.doi.org/10.1186/1752-1947-6-368 |
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author | Dell’Edera, Domenico Tinelli, Andrea Capozzi, Oronzo Epifania, Annunziata Anna Malvasi, Antonio Lofrese, Dominga Pacella, Elena Milazzo, Giusi Natalia Mazzone, Eleonora Leo, Manuela Rocchi, Mariano |
author_facet | Dell’Edera, Domenico Tinelli, Andrea Capozzi, Oronzo Epifania, Annunziata Anna Malvasi, Antonio Lofrese, Dominga Pacella, Elena Milazzo, Giusi Natalia Mazzone, Eleonora Leo, Manuela Rocchi, Mariano |
author_sort | Dell’Edera, Domenico |
collection | PubMed |
description | INTRODUCTION: Premature ovarian failure is defined as the cessation of ovarian activity before the age of 40 years. It is biochemically characterized by low levels of gonadal hormones (estrogens and inhibins) and high levels of gonadotropins (luteinizing hormone and follicle-stimulating hormone). CASE PRESENTATION: Our patient, a 22-year-old Caucasian woman under evaluation for infertility, had experienced secondary amenorrhea from the age of 18. No positive family history was noted regarding premature menopause. An examination of our patient’s karyotype showed the presence of a reciprocal translocation, apparently balanced, which had the X chromosome long arm (q13) and the 14 chromosome short arm (p12) with consequent karyotype: 46, X, t(X; 14)(q13;p12). CONCLUSIONS: Our study has underlined that karyotyping is one of the fundamental investigations in the evaluation of amenorrhea. It highlighted a genetic etiology, in the form of a chromosomal abnormality, as the causal factor in amenorrhea. |
format | Online Article Text |
id | pubmed-3520733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35207332012-12-13 Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report Dell’Edera, Domenico Tinelli, Andrea Capozzi, Oronzo Epifania, Annunziata Anna Malvasi, Antonio Lofrese, Dominga Pacella, Elena Milazzo, Giusi Natalia Mazzone, Eleonora Leo, Manuela Rocchi, Mariano J Med Case Rep Case Report INTRODUCTION: Premature ovarian failure is defined as the cessation of ovarian activity before the age of 40 years. It is biochemically characterized by low levels of gonadal hormones (estrogens and inhibins) and high levels of gonadotropins (luteinizing hormone and follicle-stimulating hormone). CASE PRESENTATION: Our patient, a 22-year-old Caucasian woman under evaluation for infertility, had experienced secondary amenorrhea from the age of 18. No positive family history was noted regarding premature menopause. An examination of our patient’s karyotype showed the presence of a reciprocal translocation, apparently balanced, which had the X chromosome long arm (q13) and the 14 chromosome short arm (p12) with consequent karyotype: 46, X, t(X; 14)(q13;p12). CONCLUSIONS: Our study has underlined that karyotyping is one of the fundamental investigations in the evaluation of amenorrhea. It highlighted a genetic etiology, in the form of a chromosomal abnormality, as the causal factor in amenorrhea. BioMed Central 2012-10-29 /pmc/articles/PMC3520733/ /pubmed/23107510 http://dx.doi.org/10.1186/1752-1947-6-368 Text en Copyright ©2012 Dell'Edera et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Dell’Edera, Domenico Tinelli, Andrea Capozzi, Oronzo Epifania, Annunziata Anna Malvasi, Antonio Lofrese, Dominga Pacella, Elena Milazzo, Giusi Natalia Mazzone, Eleonora Leo, Manuela Rocchi, Mariano Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report |
title | Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report |
title_full | Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report |
title_fullStr | Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report |
title_full_unstemmed | Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report |
title_short | Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report |
title_sort | clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old caucasian woman: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520733/ https://www.ncbi.nlm.nih.gov/pubmed/23107510 http://dx.doi.org/10.1186/1752-1947-6-368 |
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