Association of Beta-Thalassaemia and Hypogonadotropic Hypogonadism

Thalassaemic syndromes are among the most common haemoglobinopathies and are associated with high morbidity and mortality. Because of the various treatments, a secondary endocrinopathy due to iron overload—haemosiderosis—can occur, causing hypopituitarism leading to hypogonadotropic hypogonadism (HH...

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Main Authors: Angela Vidal, Carolin Dhakal
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Case Reports in Obstetrics and Gynecology
Online Access:http://dx.doi.org/10.1155/2022/4655249
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author Angela Vidal
Carolin Dhakal
author_facet Angela Vidal
Carolin Dhakal
author_sort Angela Vidal
collection DOAJ
description Thalassaemic syndromes are among the most common haemoglobinopathies and are associated with high morbidity and mortality. Because of the various treatments, a secondary endocrinopathy due to iron overload—haemosiderosis—can occur, causing hypopituitarism leading to hypogonadotropic hypogonadism (HH) and infertility. We present a case of secondary amenorrhoea in a patient with beta-thalassaemia and a history of multiple therapies in her adolescence, such as multiple transfusions, chemotherapy, and allogeneic bone marrow transplantation, who presented with HH and premature ovarian insufficiency.
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institution Kabale University
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series Case Reports in Obstetrics and Gynecology
spelling doaj-art-2e35dcd33bf34c00b30f300c3b58e8fb2025-02-03T01:20:17ZengWileyCase Reports in Obstetrics and Gynecology2090-66922022-01-01202210.1155/2022/4655249Association of Beta-Thalassaemia and Hypogonadotropic HypogonadismAngela Vidal0Carolin Dhakal1Department of Obstetrics and GynecologyDepartment of Obstetrics and GynecologyThalassaemic syndromes are among the most common haemoglobinopathies and are associated with high morbidity and mortality. Because of the various treatments, a secondary endocrinopathy due to iron overload—haemosiderosis—can occur, causing hypopituitarism leading to hypogonadotropic hypogonadism (HH) and infertility. We present a case of secondary amenorrhoea in a patient with beta-thalassaemia and a history of multiple therapies in her adolescence, such as multiple transfusions, chemotherapy, and allogeneic bone marrow transplantation, who presented with HH and premature ovarian insufficiency.http://dx.doi.org/10.1155/2022/4655249
spellingShingle Angela Vidal
Carolin Dhakal
Association of Beta-Thalassaemia and Hypogonadotropic Hypogonadism
Case Reports in Obstetrics and Gynecology
title Association of Beta-Thalassaemia and Hypogonadotropic Hypogonadism
title_full Association of Beta-Thalassaemia and Hypogonadotropic Hypogonadism
title_fullStr Association of Beta-Thalassaemia and Hypogonadotropic Hypogonadism
title_full_unstemmed Association of Beta-Thalassaemia and Hypogonadotropic Hypogonadism
title_short Association of Beta-Thalassaemia and Hypogonadotropic Hypogonadism
title_sort association of beta thalassaemia and hypogonadotropic hypogonadism
url http://dx.doi.org/10.1155/2022/4655249
work_keys_str_mv AT angelavidal associationofbetathalassaemiaandhypogonadotropichypogonadism
AT carolindhakal associationofbetathalassaemiaandhypogonadotropichypogonadism